ClinVar Miner

List of variants in gene GPD1L reported as likely benign for Brugada syndrome

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Total variants: 34
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HGVS dbSNP
NM_015141.3(GPD1L):c.*1029A>G rs6802739
NM_015141.3(GPD1L):c.*1058A>G rs79548677
NM_015141.3(GPD1L):c.*1065T>G rs6791603
NM_015141.3(GPD1L):c.*1219T>C rs2813
NM_015141.3(GPD1L):c.*1298G>A rs61392779
NM_015141.3(GPD1L):c.*132T>C rs147700828
NM_015141.3(GPD1L):c.*1472C>T rs11707908
NM_015141.3(GPD1L):c.*1473T>G rs9839305
NM_015141.3(GPD1L):c.*1828T>C rs3749278
NM_015141.3(GPD1L):c.*18G>T rs12629676
NM_015141.3(GPD1L):c.*204A>G rs6799559
NM_015141.3(GPD1L):c.*2348T>C rs3087806
NM_015141.3(GPD1L):c.*2525A>G rs7363
NM_015141.3(GPD1L):c.*300C>A rs80336593
NM_015141.3(GPD1L):c.*330C>T rs6775309
NM_015141.3(GPD1L):c.*335A>T rs6799728
NM_015141.3(GPD1L):c.*406C>G rs78129605
NM_015141.3(GPD1L):c.*505T>C rs6788436
NM_015141.3(GPD1L):c.*637C>T rs11915463
NM_015141.3(GPD1L):c.*719A>C rs11923184
NM_015141.3(GPD1L):c.*950C>T rs77308668
NM_015141.3(GPD1L):c.-119C>T rs1077601
NM_015141.3(GPD1L):c.291C>T (p.His97=) rs1007252272
NM_015141.3(GPD1L):c.366+8G>A rs72546650
NM_015141.3(GPD1L):c.396G>A (p.Lys132=) rs61741845
NM_015141.3(GPD1L):c.408C>T (p.Asp136=) rs9835387
NM_015141.3(GPD1L):c.573C>G (p.Thr191=) rs72558073
NM_015141.3(GPD1L):c.630T>C (p.Ala210=) rs373325536
NM_015141.3(GPD1L):c.691C>T (p.Arg231Cys) rs143486835
NM_015141.3(GPD1L):c.762C>T (p.Phe254=) rs1453406813
NM_015141.3(GPD1L):c.81T>C (p.Asn27=) rs34278284
NM_015141.3(GPD1L):c.837C>T (p.Phe279=) rs376724853
NM_015141.3(GPD1L):c.906G>A (p.Pro302=) rs200045526
NM_015141.3(GPD1L):c.978A>C (p.Ala326=) rs1553663699

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