ClinVar Miner

List of variants in gene GABRD reported as likely benign for EIG

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_000815.5(GABRD):c.1060-7C>T rs368961588
NM_000815.5(GABRD):c.1146C>A (p.Arg382=) rs374718450
NM_000815.5(GABRD):c.1150C>T (p.Pro384Ser) rs79386457
NM_000815.5(GABRD):c.1219G>A (p.Ala407Thr) rs143031542
NM_000815.5(GABRD):c.318C>T (p.Asn106=) rs149832567
NM_000815.5(GABRD):c.384C>T (p.Asn128=) rs767409551
NM_000815.5(GABRD):c.492C>T (p.Cys164=) rs367776284
NM_000815.5(GABRD):c.522C>T (p.Asp174=) rs534661864
NM_000815.5(GABRD):c.658C>T (p.Arg220Cys) rs139300921
NM_000815.5(GABRD):c.684C>T (p.Phe228=) rs558718893
NM_000815.5(GABRD):c.84C>T (p.Ile28=) rs769857211
NM_000815.5(GABRD):c.867G>A (p.Thr289=) rs150619024
NM_000815.5(GABRD):c.928C>T (p.Leu310=) rs745961044
NM_000815.5(GABRD):c.96G>C (p.Val32=) rs773911493

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