ClinVar Miner

List of variants in gene ABCC8 reported as benign by PreventionGenetics

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_000352.5(ABCC8):c.-19A>G rs193922394
NM_000352.5(ABCC8):c.1158C>T (p.Asn386=) rs60824529
NM_000352.5(ABCC8):c.1572G>A (p.Thr524=) rs61748766
NM_000352.5(ABCC8):c.1686C>T (p.His562=) rs1799857
NM_000352.5(ABCC8):c.1926C>G (p.Pro642=) rs75376282
NM_000352.5(ABCC8):c.1947G>A (p.Lys649=) rs1799858
NM_000352.5(ABCC8):c.207T>C (p.Pro69=) rs1048099
NM_000352.5(ABCC8):c.2117-3C>T rs1799854
NM_000352.5(ABCC8):c.2277C>T (p.Thr759=) rs1801261
NM_000352.5(ABCC8):c.2485C>T (p.Leu829=) rs1805036
NM_000352.5(ABCC8):c.2538C>T (p.His846=) rs73423037
NM_000352.5(ABCC8):c.2820+17A>G rs2106865
NM_000352.5(ABCC8):c.330C>T (p.Ala110=) rs8192695
NM_000352.5(ABCC8):c.3329+6C>T rs113873225
NM_000352.5(ABCC8):c.354C>T (p.Val118=) rs137873871
NM_000352.5(ABCC8):c.3612C>T (p.Ala1204=) rs149861153
NM_000352.5(ABCC8):c.3819G>A (p.Arg1273=) rs1799859
NM_000352.5(ABCC8):c.4105G>T (p.Ala1369Ser) rs757110
NM_000352.5(ABCC8):c.4120-19C>T rs1800853
NM_000352.5(ABCC8):c.423G>A (p.Val141=) rs116132921
NM_000352.5(ABCC8):c.4542C>A (p.Ala1514=) rs113282901
NM_000352.5(ABCC8):c.579+14C>T rs2301703
NM_000352.5(ABCC8):c.822+20C>T rs181998151

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