ClinVar for Gene (Select 7482) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190727	NM_024494.3(WNT2B):c.983C>T (p.Thr328Ile)	ST7L, WNT2B (T236I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190726	NM_024494.3(WNT2B):c.967C>T (p.Arg323Cys)	ST7L, WNT2B (R231C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190725	NM_024494.3(WNT2B):c.94G>C (p.Gly32Arg)	LOC122094899, WNT2B (G32R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190724	NM_024494.3(WNT2B):c.668G>A (p.Arg223His)	WNT2B (R131H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190723	NM_024494.3(WNT2B):c.314G>A (p.Arg105Gln)	WNT2B (R13Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190722	NM_024494.3(WNT2B):c.1097G>A (p.Arg366Gln)	ST7L, WNT2B (R366Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2958271	NM_024494.3(WNT2B):c.291C>T (p.Gly97=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2908726	NM_024494.3(WNT2B):c.1017C>T (p.Cys339=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2908630	NM_024494.3(WNT2B):c.948T>C (p.Gly316=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2905444	NM_024494.3(WNT2B):c.1032C>T (p.Tyr344=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2897258	NM_024494.3(WNT2B):c.822G>A (p.Gln274=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2888002	NM_024494.3(WNT2B):c.1173C>G (p.Thr391=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880188	NM_024494.3(WNT2B):c.885C>T (p.Thr295=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877051	NM_024494.3(WNT2B):c.9A>G (p.Arg3=)	LOC129931208, WNT2B	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2876619	NM_024494.3(WNT2B):c.150G>A (p.Leu50=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2869382	NM_024494.3(WNT2B):c.182+15C>A	LOC122094899, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867647	NM_024494.3(WNT2B):c.102G>A (p.Arg34=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2862160	NM_024494.3(WNT2B):c.153G>T (p.Thr51=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2850986	NM_024494.3(WNT2B):c.504T>C (p.Cys168=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2841916	NM_024494.3(WNT2B):c.1062G>A (p.Gln354=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2841399	NM_024494.3(WNT2B):c.946+17G>A	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2819968	NM_024494.3(WNT2B):c.12G>A (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2810135	NM_024494.3(WNT2B):c.54C>G (p.Ala18=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2800852	NM_024494.3(WNT2B):c.745C>T (p.Arg249Cys)	WNT2B (R157C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2800402	NM_024494.3(WNT2B):c.861C>A (p.Ala287=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2796114	NM_024494.3(WNT2B):c.799C>T (p.Arg267Ter)	WNT2B (R175* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2795858	NM_024494.3(WNT2B):c.90C>T (p.Pro30=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2793117	NM_024494.3(WNT2B):c.947-18C>T	ST7L, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2776256	NM_024494.3(WNT2B):c.69T>C (p.Pro23=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2776011	NM_024494.3(WNT2B):c.12G>C (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2759047	NM_024494.3(WNT2B):c.946+17G>C	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2745879	NM_024494.3(WNT2B):c.126C>G (p.Ala42=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2743128	NM_024494.3(WNT2B):c.1143C>T (p.Ala381=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2742722	NM_024494.3(WNT2B):c.645C>T (p.Ala215=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2741236	NM_024494.3(WNT2B):c.468C>G (p.Arg156=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2730090	NM_024494.3(WNT2B):c.969T>C (p.Arg323=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2728592	NM_024494.3(WNT2B):c.819G>A (p.Val273=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2727253	NM_024494.3(WNT2B):c.816T>A (p.Ala272=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2712168	NM_024494.3(WNT2B):c.1096C>A (p.Arg366=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2710362	NM_024494.3(WNT2B):c.1158G>A (p.Glu386=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2704878	NM_024494.3(WNT2B):c.324G>A (p.Gln108=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2704273	NM_024494.3(WNT2B):c.855C>T (p.Thr285=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693015	NM_024494.3(WNT2B):c.914C>T (p.Ser305Phe)	WNT2B (S286F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2685577	GRCh37/hg19 1p13.3-13.1(chr1:110066946-116672408)x1	ADORA3, AHCYL1 +77 more	Copy number loss	not provided	GPathogenic
Select item 2536566	NM_024494.3(WNT2B):c.1033G>A (p.Asp345Asn)	ST7L, WNT2B (D345N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516583	NM_024494.3(WNT2B):c.79C>T (p.Pro27Ser)	LOC122094899, WNT2B (P27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493435	NM_024494.3(WNT2B):c.994A>G (p.Thr332Ala)	ST7L, WNT2B (T240A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425617	NC_000001.10:g.(?_112318699)_(115576848_?)del	CSDE1, AP4B1 +28 more	Deletion	Hereditary spastic paraplegia 47	GPathogenic
Select item 2424614	NC_000001.10:g.(?_111145905)_(114454813_?)del	DDX20, LRIF1 +34 more	Deletion	not provided	GPathogenic
Select item 2325715	NM_024494.3(WNT2B):c.692G>C (p.Arg231Pro)	WNT2B (R212P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320366	NM_024494.3(WNT2B):c.1159T>C (p.Trp387Arg)	ST7L, WNT2B (W387R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309266	NM_024494.3(WNT2B):c.65T>C (p.Val22Ala)	LOC122094899, WNT2B (V22A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308739	NM_024494.3(WNT2B):c.551A>C (p.Asp184Ala)	WNT2B (D165A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241026	NM_024494.3(WNT2B):c.602C>T (p.Ala201Val)	WNT2B (A109V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2193275	NM_024494.3(WNT2B):c.621G>T (p.Glu207Asp)	WNT2B (E115D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2190366	NM_024494.3(WNT2B):c.368G>A (p.Arg123Gln)	WNT2B (R104Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2183279	NM_024494.3(WNT2B):c.201G>A (p.Gly67=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2179278	NM_024494.3(WNT2B):c.802C>T (p.Arg268Cys)	WNT2B (R268C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2178300	NM_024494.3(WNT2B):c.334C>T (p.Arg112Cys)	WNT2B (R93C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2173640	NM_024494.3(WNT2B):c.456C>T (p.His152=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2173050	NM_024494.3(WNT2B):c.888G>A (p.Arg296=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2170828	NM_024494.3(WNT2B):c.1000G>A (p.Gly334Ser)	ST7L, WNT2B (G334S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2163807	NM_024494.3(WNT2B):c.289G>A (p.Gly97Ser)	WNT2B (G78S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2154862	NM_024494.3(WNT2B):c.539G>A (p.Arg180His)	WNT2B (R161H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2139654	NM_024494.3(WNT2B):c.377C>G (p.Thr126Ser)	WNT2B (T126S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2132434	NM_024494.3(WNT2B):c.250C>T (p.Gln84Ter)	WNT2B (Q84* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2127316	NM_024494.3(WNT2B):c.158C>G (p.Pro53Arg)	LOC122094899, WNT2B (P53R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2123833	NM_024494.3(WNT2B):c.182+8del	LOC122094899, WNT2B	Deletion (intron variant)	not provided	GLikely benign
Select item 2123032	NM_024494.3(WNT2B):c.929T>A (p.Val310Asp)	WNT2B (V310D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2119068	NM_024494.3(WNT2B):c.11C>T (p.Pro4Leu)	LOC129931208, WNT2B (P4L)	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 2116080	NM_024494.3(WNT2B):c.1172C>A (p.Thr391Asn)	ST7L, WNT2B (T299N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2113841	NM_024494.3(WNT2B):c.760G>A (p.Ala254Thr)	WNT2B (A235T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2112949	NM_024494.3(WNT2B):c.199G>T (p.Gly67Trp)	WNT2B (G67W +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2107953	NM_024494.3(WNT2B):c.252G>C (p.Gln84His)	WNT2B (Q65H +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2100215	NM_024494.3(WNT2B):c.23A>C (p.Glu8Ala)	LOC129931208, WNT2B (E8A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2086741	NM_024494.3(WNT2B):c.47G>C (p.Arg16Pro)	LOC122094899, LOC129931208 +1 more (R16P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2085920	NM_024494.3(WNT2B):c.582C>T (p.Tyr194=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2083761	NM_024494.3(WNT2B):c.816T>C (p.Ala272=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2074796	NM_024494.3(WNT2B):c.404-11TC[3]	WNT2B	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2071445	NM_024494.3(WNT2B):c.877C>T (p.Arg293Cys)	WNT2B (R201C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070210	NM_024494.3(WNT2B):c.779G>A (p.Arg260His)	WNT2B (R241H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070181	NM_024494.3(WNT2B):c.723C>T (p.Gly241=)	WNT2B	Single nucleotide variant (synonymous variant)	WNT2B-related disorder +1 more	GLikely benign
Select item 2068511	NM_024494.3(WNT2B):c.601G>T (p.Ala201Ser)	WNT2B (A182S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2065166	NM_024494.3(WNT2B):c.1142C>T (p.Ala381Val)	WNT2B, ST7L (A362V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2062623	NM_024494.3(WNT2B):c.176C>G (p.Ser59Cys)	LOC122094899, WNT2B (S59C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2057211	NM_024494.3(WNT2B):c.468C>T (p.Arg156=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2056303	NM_024494.3(WNT2B):c.642G>A (p.Arg214=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2055556	NM_024494.3(WNT2B):c.151A>G (p.Thr51Ala)	LOC122094899, WNT2B (T51A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2054128	NM_024494.3(WNT2B):c.603C>T (p.Ala201=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045490	NM_024494.3(WNT2B):c.457G>A (p.Ala153Thr)	WNT2B (A61T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2041928	NM_024494.3(WNT2B):c.1059C>G (p.Thr353=)	ST7L, WNT2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2040803	NM_024494.3(WNT2B):c.1126G>A (p.Val376Ile)	WNT2B, ST7L (V357I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2038351	NM_024494.3(WNT2B):c.947-16C>G	ST7L, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2033044	NM_024494.3(WNT2B):c.404-6C>A	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2031611	NM_024494.3(WNT2B):c.426A>G (p.Val142=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2025024	NM_024494.3(WNT2B):c.228T>C (p.Pro76=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2019807	NM_024494.3(WNT2B):c.719A>G (p.His240Arg)	WNT2B (H148R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2018411	NM_024494.3(WNT2B):c.321T>C (p.Cys107=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2013692	NM_024494.3(WNT2B):c.139CTG[5] (p.Leu50_Thr51insLeu)	LOC122094899, WNT2B	Microsatellite (inframe_insertion +1 more)	not provided	GUncertain significance
Select item 2003996	NM_024494.3(WNT2B):c.351C>T (p.Asn117=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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