List of variants in gene ADAR reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.1926T>C (p.His642=)	rs150171059	0.00132
NM_001111.5(ADAR):c.3018C>T (p.Asn1006=)	rs151241634	0.00063
NM_001111.5(ADAR):c.3523A>C (p.Arg1175=)	rs146625055	0.00042
NM_001111.5(ADAR):c.2052G>A (p.Ala684=)	rs148041309	0.00038
NM_001111.5(ADAR):c.1934+8C>T	rs376025865	0.00013
NM_001111.5(ADAR):c.2274C>T (p.Phe758=)	rs149039619	0.00011
NM_001111.5(ADAR):c.222G>A (p.Arg74=)	rs150423721	0.00010
NM_001111.5(ADAR):c.1392T>C (p.Asn464=)	rs370763473	0.00009
NM_001111.5(ADAR):c.1890C>T (p.Cys630=)	rs558496566	0.00007
NM_001111.5(ADAR):c.1875A>G (p.Lys625=)	rs771871176	0.00006
NM_001111.5(ADAR):c.3171G>A (p.Leu1057=)	rs149496690	0.00006
NM_001111.5(ADAR):c.57C>T (p.Gly19=)	rs137983302	0.00006
NM_001111.5(ADAR):c.1192A>G (p.Asn398Asp)	rs371050239	0.00005
NM_001111.5(ADAR):c.3289C>A (p.His1097Asn)	rs200537032	0.00003
NM_001111.5(ADAR):c.624C>T (p.Ser208=)	rs755808579	0.00002
NM_001111.5(ADAR):c.1158C>T (p.Asn386=)	rs752276168	0.00001
NM_001111.5(ADAR):c.1189T>A (p.Ser397Thr)	rs1190740301	0.00001
NM_001111.5(ADAR):c.30C>T (p.Ser10=)	rs769752403	0.00001
NM_001111.5(ADAR):c.474A>C (p.Ala158=)	rs1434133622	0.00001
NM_001111.5(ADAR):c.999G>A (p.Val333=)	rs781217449	0.00001
NM_001111.5(ADAR):c.2262C>T (p.His754=)	rs779685414
NM_001111.5(ADAR):c.3234T>C (p.Arg1078=)	rs2526457623

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