"XIST-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042649	NR_001564.2(XIST):n.18978T>C	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038264	NR_001564.2(XIST):n.18167A>T	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3048676	NR_001564.2(XIST):n.17820C>T	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3045578	NR_001564.2(XIST):n.16850A>C	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3045837	NR_001564.2(XIST):n.16120T>A	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038685	NR_001564.2(XIST):n.16106del	TSIX, XIST	Deletion (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3039573	NR_001564.2(XIST):n.12197G>A	TSIX, XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3040534	NR_001564.2(XIST):n.10571T>C	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3032664	NR_003255.1(TSIX):n.18379_18389delTGTATCCTGGC	XIST	Deletion (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3041442	NR_001564.2(XIST):n.10270C>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3039016	NR_001564.2(XIST):n.10134T>C	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038835	NR_001564.2(XIST):n.10121A>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3039258	NR_001564.2(XIST):n.9928T>C	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3040456	NR_001564.2(XIST):n.9755C>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3034421	NR_003255.1(TSIX):n.19801_19802delAC	XIST	Deletion (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3056865	NR_001564.2(XIST):n.8678A>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3045435	NR_001564.2(XIST):n.7933A>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3041667	NR_001564.2(XIST):n.6429C>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3043452	NR_001564.2(XIST):n.6356C>A	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3034118	NR_001564.2(XIST):n.5093A>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3037539	NR_001564.2(XIST):n.4934C>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3038647	NR_001564.2(XIST):n.4158T>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038410	NR_001564.2(XIST):n.4016A>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3055882	NR_001564.2(XIST):n.2848C>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3050691	NR_001564.2(XIST):n.2735G>A	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3039382	NR_001564.2(XIST):n.2339G>A	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038232	NR_001564.2(XIST):n.2326A>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3040467	NR_001564.2(XIST):n.2092A>C	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3041443	NR_001564.2(XIST):n.2053C>G	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GLikely benign
Select item 3035143	NR_001564.2(XIST):n.945G>A	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3037804	NR_001564.2(XIST):n.649A>T	XIST	Single nucleotide variant (non-coding transcript variant)	XIST-related condition	GBenign
Select item 3038714	NR_003255.1(TSIX):n.28288_28289delAA	XIST	Deletion (non-coding transcript variant)	XIST-related condition	GLikely benign

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Items: 32