ClinVar for MedGen (Select 48574) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065824	NM_023004.6(RTN4R):c.1130G>A (p.Arg377Gln)	RTN4R (R377Q)	Single nucleotide variant (missense variant)	Schizophrenia	GUncertain significance
Select item 2920607	NM_001044.5(SLC6A3):c.950_989del	SLC6A3	Deletion (3 prime UTR variant)	Schizophrenia	GUncertain risk allele
Select item 2920606	NM_001044.5(SLC6A3):c.419-3595A>T	SLC6A3	Single nucleotide variant (intron variant)	Schizophrenia	GBenign
Select item 2920605	NC_000005.10:g.1448033A>G	SLC6A3	Single nucleotide variant	Schizophrenia	GBenign
Select item 2507407	NM_000798.5(DRD5):c.978C>T (p.Pro326=)	DRD5, SLC2A9	Single nucleotide variant (synonymous variant)	Schizophrenia +1 more	GUncertain significance
Select item 2505115	NM_015080.4(NRXN2):c.5038_5039del (p.Ser1680fs)	NRXN2 (S1449fs +9 more)	Deletion (frameshift variant)	Autism spectrum disorder +1 more	Gnot provided
Select item 1801470	NC_000002.12:g.239925792_239928083del	NDUFA10	Deletion (genic downstream transcript variant)	Schizophrenia	GUncertain significance
Select item 1801469	NM_000489.6(ATRX):c.4557+897_4557+898insTGTTTTTTTTTTTTTTTTTGTAGTTTTTTTTTTTTTTTTGTGTG	ATRX	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801468	NM_004006.3(DMD):c.94-29188_94-29187insTTTTTTTTTTTTTCTGGGGTTTTTTTTTTTTTTTGGATG	DMD	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801467	NM_001887.4(CRYBB1):c.575+231_575+232insAGAGCCTTACCGAGTCTTATGTCCTACTGACCTTGGAAAACGTCCGAACTGTTTCCCCCCCTCTGATTCTCGTTTGCTCGACGCACCTAGAATACAGGTGACCCGTACGGGAGGTGGGATGGAGTCTGTGTGTCCGACTGTATCCCGTTGGTGAGACGGGTTGTCCCTGAACCTGATAGGGACAAAATATACCTCAGTGATTCCCGGGTCTCTGTTGGTGTCTCCCTGTCCTTGTCCGTCACAATTCGTAACCACTAGTAATTCTCGAAGTCAATCCTTACTTGATGTTAGTTAGAACTCAAGCTTAGTACGACACGGTGAATGGTTTATCCACA	CRYBA4, CRYBB1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801466	NM_002240.5(KCNJ6):c.947-6762_947-6761insGTTTGTTTGTGGTGTGTGTTTTTTGTTGTTGGAGACGGAGTTCTCGCTCTGTCGGCCCTAGGCCGCGACGGCGGACTGCAGTGGCGCAATCTAGTGCGCCAGCTGCAAGCTCCGCTGGCCGGGGTGCACGCACTCTATTTCTCCTGTCCTCTAGCCTGCCCGGAGTAGCTGGGAACTACAGGCGCCCGCCACTGCGCCCGGCTAATGTGTGGAGTTTTTAGTAGAGGAGGGGGGTCACCTTGTTGTGAGACAGGATATGGTGTCTGCGATCTCGGACCTCATGATACACCCGCCTAACGGCTCCAAAGTGCGGGGCTGACAGGCGTGGCCAACGCGCTTCCGGCCCGGCC	KCNJ6, KCNJ6-AS1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801465	NM_000178.4(GSS):c.129+1703_129+1704insTATGTGTGTGTGTGTGTGTGTGTTGTGTGTGTGGTGTGTGTGTTCGTTC	GSS	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801464	NM_176787.5(PIGN):c.2673-514_2673-513insGCAAACCGGCCGGGCGGTGGCTGACGCCCTGTAATCCCAGCACTTTGGCAAAAGAAGGCCGAGGCGGGCGGATCACGAGGGTCAGGATATCGAGACAATTCCGGCTCTAAAACGGTGAAACCTCGTTCTATAAAAATATACCAAAACAATTAGACGGGCGTTGTGGCGGGCGCCTGTAAGTCCAGCTACCTTGGGAGGTGAGGCAGGAGAATGGCGTGAACCCGGGAGGGCGGAGCTTGCAGTCTGAGACGAGATCCCGCCACTGCACACAGCGCTGGGCGACAGAGCGCGAGACCCTCCGTCTCAAAAAAAAAAAAAAAAAAAGAAGTGT	PIGN	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801463	NM_016373.4(WWOX):c.1056+95264_1056+95265insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	WWOX	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801462	NM_020843.4(SCAPER):c.3311+2919_3311+2920insTTTACACTTTTACTAAATTTTAATTTAAAATTTAGTAAATTAAAATAAAATTTTACTATTTTTAATTAGGCTTGTTTTACACTTGGGTTTTTT	SCAPER	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801461	NM_013243.4(SCG3):c.398-1539_398-1538insCAACTGCAACTGGCTGGTGGACTTGGAACTTTTTTTTCTCTCACTTGCCTGGAAAAGTGCAAGGCAAGAACCTGAGAAACGAGCCTGTTATGCAGACCCAAATCATCCTTGCGATGGGCTGTT	SCG3	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801460	NC_000002.12:g.239921648_239921688del	NDUFA10	Deletion (genic downstream transcript variant)	Schizophrenia	GUncertain significance
Select item 1801459	NM_002576.5(PAK1):c.1551+376_1551+377insCTTCGCTTCCCCTCCAATCCTTCCCTTCCTTCCCCTCCTCCTACCCCCTCCCCTCCCCCTCCCCCTCCCCCTCCCCCCTCCCTCCCCCCTCCCCTCTCCCCTTCCCCCTCCCCTCCCCCCTCCCCTCCCCTCCCCTTCCCCACCCTCCCCCCCTCCCCTCCCCTCCCCTCCCC	PAK1	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801458	NM_018026.4(PACS1):c.2430-649_2430-648insCTTTCTTTGGTTTGTTTTTGTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGGAAGTGCAGTGGCGGCGATCTCGGGCTCACTGCAAGCTCCGCCTCCCGGGTGTTCACGCCATTCTCCGCCTCAGCCATCCAAAGTAGAGCGGACTAAGGCGCCGCCACTACGCCCGAGCTAATTTTTTTGTATTTTTAGTTAGAGACGGGGTTTCACCGTTTTAGCCGGGATGGTCTCGATACTCCTGACTCGTGATCCGCCCGCCTGCCTCCCAAAGTGCTGGAGGATTTACAGCGGGCCACCGCTGCCCGGCCTAA	PACS1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801457	NM_000507.4(FBP1):c.171-4630_171-4629insTCACTTTATTTTATTTTTTTTTTTTTGGAGACGGGAAGTCTCGCTTGTCGCCAGGATGGAGTGCAGTGGCGCAATCTCGGCTCAATGCAGGCTCCGACCCCCTGGGGTTCACGCCATTCTCCTGCCTGCAGACTCCGAGTAGCTGGGACTACAGGCGCCCGCCCACTCGCCCGGCTAATTTTTTTGTGTATTTTTAGTAGAGACGGGGTTCACCGTTGTGTTGAGCCAGGATGGTCTCGATCTCCCTGACCTCGGCTCCGCCCGTATCTTCGGGACTCCCAAAGTGTGGAGAGATTACAGGCGTGAGCCACCGCGGCCACGGCCTA	FBP1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801456	NM_000443.4(ABCB4):c.135+3688_135+3689insTTTATTTATTTTATTTTATTTTATATTATTTTTATCTTAT	ABCB4	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801455	NM_012301.4(MAGI2):c.301+85161_301+85162insAATCAATTAAAAAATATATATATATATAATATATACTATATATATACAATCGATATAG	MAGI2	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801454	NM_001166412.2(SMOC2):c.907+15386_907+15387insTGTAATTACTACCAGCGTGGAATAAAAACACC	SMOC2	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801453	NM_001374828.1(ARID1B):c.2248-8118_2248-8117insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGCGTTCCTCGCTCTGTCTCCCCAAGGTCGTACTGCGACTGCAGTGGCGCAATCTCGGCTCACTGCCAAGCTCCGCTTCCCCGGGTTCACGCCATTCTCCGCCTCAGCTCCCGAGTAGCTGGGACTACAGGCGCCGCCACCGCGCCCGGCTAATTTTTTGTAATTTTTTAGTAGGAACGGTGTTCAGACTTGTTAGCCAGGATGGTCTCGATCTCCTGACCCATTTAGGCTCATGATCCACCCGCCTCGGCTCCGCAAGGTGCTGGTATTACAGCGTGAGCCACCGCGCCCGGGGCCCTTCATGT	ARID1B	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801452	NM_000426.4(LAMA2):c.8704-401_8704-400insAAAATTGGGCCCCCCTGGGCGCGGTGGATCAAGCCTGTAATCCAGCACTTTGGGAGGGCCGAGGCCGGCGGATCCGAGGTCAGGAGATCCGAGACCATCCGAGCTAAAACGGTGAATTGAAACCCCGTCTTACTAAAAAATTACAAAAATTAGTCCGGGCTAGTGGCGGGCGATGTAGTCCAGCTACTGGGAGGCTGAGGCAGGAGAATGGCCCAGGGGAAACCCGGGAGGCGGGAGCTTGCAGAGCTGAGCCGAGGTCCCCGCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	LAMA2	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801451	NM_000046.5(ARSB):c.691-2429_691-2428insTGATAATCGATGTTACACTTTATAGAAAGAATATGATAAAAAATTTAACTTTTTTTTCTCTTTTCTCGATCACAAAAAGTGTATGAATACCGAGTATCGTAATCACCTATACTTAAATTGAATCCTGAGTTTCCACAGAGGTTAGTGTCACAAACCCTGGGGTGACGTCGTGTGTCAGTGGATCCTTGGACGGAGTCTCACTTGTCAGACACCAGTTAAAGGGTGTGAGGGATTTCAGGTTTGTCTTACTGAGTGCCGAGTGTTGACAGTCGGGATTTCGGTCGTCGACTCGGTAGTGCCTCGGGACTAGAGTAGGTGGGACGAAAAAGAGATCCAGGTCTAGGAAACTAGGAAA	ARSB	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801450	NM_000949.7(PRLR):c.374-1769_374-1768insATATATATATATATTATATATATATCTATATATTATAT	PRLR	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801449	NM_005235.3(ERBB4):c.82+91828_82+91864del	ERBB4	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801448	NM_001364905.1(LRBA):c.7195-22597_7195-22596insGCTGGTCGGCGGTGGCTCACGCCTGTAATCCAGCACTTTGGGGAGGCTCGAGCGGGCTGGATCAAAGGTCAGGAGATCGTGTGACCATCTTGGCTAACAACGGTTAAGCCACCGTCTCTTACAAAATACAAAAATTATCCGGGCGCGTGGCGGGCGCCTGTAGTCCCGCAGCTACTCGGGAGGCTGAGGCGGAAGAATGGCGTGAACCTGGGAGGCGTGAAGCTTGCAGTGACCGAGATGTGGTGTCGCCACTGCAATCCGGCCTGGCTAACCGAGCGGACTCCAGTCTCAAAAAAAAAAATAAAAAAAACAAAAAAAAAAAAAAGAACTTACTAA	LRBA	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801447	NM_001080476.3(GRXCR1):c.384+27065_384+27066insTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTGAGACGGAGTTCTCGCTCTGAGCCAAGGCTGTGGCAGTGCAGTGGCGGGATATCGGCTCACTGCAAGCCTCCGGCCTCGGTCACGCCATTCCTCCTGCCCTCAGCCTCCCCCACGTGTAGTGGGATACAGGCGCCCCGCCCACTACGCTCCGGTAATTTTTGTATTTTTTTGTAGTAGAGACGGGGGGTTTCACCGTTTTTAGCAGGGATGGGTCTCGATCTCCTGACCTCGTCTGATCGCCCGCCTCGGACTCCCAAAGTGCTGGGGATTACAGCGTGTCGAGCCACCGCGCACGGCATAA	GRXCR1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801446	NM_020041.3(SLC2A9):c.682-8847_682-8846insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	SLC2A9	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801445	NM_001271838.2(RSRC1):c.652+16796_652+16797insCTCTTTATATAGTCTATATCTATAATTACTATACTATATT	RSRC1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801444	NM_000404.4(GLB1):c.1068+2341_1068+2342insGCTTGGTATTTTTTCTGAGGGTATCTTTGCTTGGTATTTTTCTGAGTTAGCTTTTGCTTGTATTTTTTTTTCTGATGTACTTT	GLB1	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801443	NM_001267550.2(TTN):c.10679-350_10679-349insCAAAGTAAGCTTAAAGTCTTACTATGCACCTTAAAGTAAGTACAAGTATACTACTGCACTTAAAGTAAGTAAAGTATTAAGTGCCACTTAAAGTAAGTACAGTATACGTACTGCCCACCTTAAAGTAAGTACAGTATACTTACTCGCCCCTTAAAGTAAGCTCCGCAGTATACTACTGCACTAAAAGTAAGTACAGTATTACTTCTGCACTAAAGTAAGTACAAGTCATACTTACTAGTACGTAAAGAAGTACAGTATACTCTGATACTTAAAGTAAGACAGCTATTAACTTACTGTACTTAAGTAAGTCCAGTATTACTTACGGTACTTAAGTAAGTACAGTCTTTTATGTTATTTGAGCGGTACTTAAGTAAGTACAGTATTATTACTGTACATTTGAGCGGTACTTAAGTAAGTACAGTATTATTACTGTA	TTN	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801442	NM_001287491.2(TET3):c.361-13808_361-13807insTTGTGTGTTGGTCGTGTGCGCGCGCCCCCCGCTCCCGCGCGCGATGGCCCAGCGGCTGGCAAGAGGGTGTGTGT	TET3	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801441	NM_015189.3(EXOC6B):c.2197-66917_2197-66916insTAAATATATTTTAATTAAATTACATTATTAAATATCAATCAG	EXOC6B	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801440	NM_138801.3(GALM):c.553-3587_553-3586insCCTTCCTTCCTTCCTTCGCTTTCCCTTCGCTTCCTTCCTTCCCTTCCTTCT	GALM	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801439	NM_015909.4(NBAS):c.3590+180_3590+181insTTGCTTTTTTTTTTTTTTTTTGAGTACGTGAAGTCTCGCTCTGTCCGCACAGGATGGAGTGCAGTGGCGCGATTTCTCGCTCCCTGCAAGCTGCCGACCTCCCGGGTCACGCCATCTCCTGCCTCAGCCTCCCGAGCTAGCTGGGGCTACAGGCGCCCGCTACCACGCACGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTAGCCAGGATGGTCTCGATACGCCTAGACCTCGTGATCCGCCCGCCTCGCCTCCAAAGTGCTGTGGATTACAGGCGTACCACCCGCGCACCCCCGGCCCCATCAGCTTC	NBAS	Insertion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801438	NM_005235.3(ERBB4):c.421+36999_421+40917del	ERBB4	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801437	NM_000489.6(ATRX):c.5135-5541_5135-5497del	ATRX	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801436	NM_014271.4(IL1RAPL1):c.779-114287_779-114141del	IL1RAPL1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801435	NM_001353214.3(DYM):c.764-3174_764-3107del	DYM	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801434	NM_001378183.1(PIEZO2):c.287-33303_287-33270del	PIEZO2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801433	NM_001372.4(DNAH9):c.2595+1072_2595+1392del	DNAH9	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801432	NM_016373.4(WWOX):c.1056+186391AT[7]	WWOX	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801431	NM_000336.3(SCNN1B):c.-8-15491_-8-15437del	SCNN1B	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801430	NM_144672.4(OTOA):c.1105-2294TTTC[6]	OTOA	Microsatellite (intron variant)	Schizophrenia	GUncertain significance
Select item 1801429	Single allele	SCAPER	Deletion	Schizophrenia	GUncertain significance
Select item 1801428	NM_004998.4(MYO1E):c.3081-906_3081-872del	MYO1E	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801427	NM_001130987.2(DYSF):c.5318-76_5318-44del	DYSF	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801426	NM_005739.4(RASGRP1):c.221-16458_221-16419del	RASGRP1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801425	NM_000810.4(GABRA5):c.497+8842_497+8896del	GABRA5	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801424	NM_000814.6(GABRB3):c.240+8206_240+8254del	GABRB3	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801423	NM_004184.4(WARS1):c.827-1253_827-1215del	WARS1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801422	NM_020806.5(GPHN):c.828+16787_828+16846del	GPHN	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801421	NM_207361.6(FREM2):c.6019+20342_6019+24474del	FREM2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801420	NM_004984.4(KIF5A):c.130-5236_130-4967del	KIF5A	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801419	NM_021957.4(GYS2):c.122-3879_122-3845del	GYS2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801418	NM_032801.5(JAM3):c.76+25456_76+25517del	JAM3	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801417	NM_001012393.5(OPCML):c.62-182699_62-182663del	OPCML	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801416	NM_033109.5(PNPT1):c.1496-3539_1496-3401del	PNPT1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801415	NM_004771.4(MMP20):c.953+5103_953+5414del	MMP20	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801414	NM_017635.5(KMT5B):c.-76-8323_-76-8288del	KMT5B	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801413	NM_000314.8(PTEN):c.165-8956_165-8924del	PTEN	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801412	NM_001354404.2(PCDH15):c.-156+225495_-156+225533del	PCDH15	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801411	NM_006258.4(PRKG1):c.592+85868_592+85928del	PRKG1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801410	NM_014317.5(PDSS1):c.467+307_467+3456del	PDSS1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801409	NM_001370100.5(ZMYND11):c.438+4276_438+4325del	ZMYND11	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801408	NM_020822.3(KCNT1):c.760-365_760-232del	KCNT1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801407	NM_001369458.1(NFIB):c.96+33125_96+33183del	NFIB	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801406	NM_015158.5(KANK1):c.38-3358_38-2787del	KANK1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801405	NM_201253.3(CRB1):c.989-2014_989-1973del	CRB1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801404	NM_014141.6(CNTNAP2):c.1498+47142_1498+47201del	CNTNAP2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801403	NM_014141.6(CNTNAP2):c.1348+54355_1348+54568del	CNTNAP2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801402	NM_000492.4(CFTR):c.3367+201_3367+243del	CFTR, LOC111674472	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801401	NM_198428.3(BBS9):c.1017-27152_1017-27053del	BBS9	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801400	NM_004067.4(CHN2):c.88+5444_88+5482del	CHN2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801399	NM_004067.4(CHN2):c.49+68970_49+69013del	CHN2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801398	NM_017802.4(DNAAF5):c.2432-276_2432-199del	DNAAF5	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801397	NM_004562.3(PRKN):c.171+62801_171+62835del	PRKN	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801396	NM_004562.3(PRKN):c.734+77606_734+77826del	PRKN	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801395	NM_001128164.2(ATXN1):c.-160-39282_-160-39238del	ATXN1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801394	NM_177398.4(LMX1A):c.263+5059_263+5145del	LMX1A	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801393	NM_030948.6(PHACTR1):c.1391+978_1391+1218del	PHACTR1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801392	NM_006567.5(FARS2):c.1218-32980_1218-32942del	FARS2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801391	NM_024577.4(SH3TC2):c.3675+505_3675+604del	SH3TC2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801390	NM_001903.5(CTNNA1):c.-2-5766_-2-5573del	CTNNA1	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801389	NM_024867.4(SPEF2):c.3064-5518_3064-5480del	SPEF2	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801388	NM_000949.7(PRLR):c.373+637_373+688del	PRLR	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801387	NM_004174.4(SLC9A3):c.212-5768_212-5635del	SLC9A3	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801386	NM_000222.3(KIT):c.1231+2109_1231+2185del	KIT	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801385	NM_001374401.1(RBPJ):c.-166-73601_-166-68683del	LOC129992362, RBPJ	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801384	NM_015141.4(GPD1L):c.225+2463_225+2505del	GPD1L	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1801383	NM_014762.4(DHCR24):c.876+2630_876+2682del	DHCR24	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1709227	NM_133625.6(SYN2):c.1585C>T (p.Gln529Ter)	SYN2 (Q529*)	Single nucleotide variant (nonsense)	Schizophrenia	GUncertain significance
Select item 1672993	NM_001382430.1(AKT1):c.634-13C>T	AKT1	Single nucleotide variant (intron variant)	Schizophrenia +1 more	GBenign/Likely benign
Select item 1445361	NM_005957.5(MTHFR):c.203G>A (p.Arg68Gln)	MTHFR (R109Q +1 more)	Single nucleotide variant (missense variant)	Homocystinuria due to methylene tetrahydrofolate reductase deficiency +3 more	GUncertain significance
Select item 1369489	NM_005957.5(MTHFR):c.673A>G (p.Ile225Val)	MTHFR (I225V +1 more)	Single nucleotide variant (missense variant)	Schizophrenia +4 more	GConflicting classifications of pathogenicity
Select item 1339872	GRCh37/hg19 3p25.3-25.2(chr3:10970972-12295919)x1	TIMP4, VGLL4 +6 more	Copy number loss	Schizophrenia	Gnot provided
Select item 1339462	NM_017934.7(PHIP):c.4174_4175insATTTTCAGTAATTATTTTCAGTAATT (p.Ser1392delinsTyrPheGlnTer)	IRAK1BP1, PHIP	Microsatellite (nonsense)	Schizophrenia	GPathogenic

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