ClinVar Miner

List of variants in gene ABCC8 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_000352.6(ABCC8):c.-19A>G rs193922394
NM_000352.6(ABCC8):c.-49G>C rs77498130
NM_000352.6(ABCC8):c.-8G>T rs200091822
NM_000352.6(ABCC8):c.105G>A (p.Pro35=) rs199925058
NM_000352.6(ABCC8):c.1158C>T (p.Asn386=) rs60824529
NM_000352.6(ABCC8):c.1252T>C (p.Cys418Arg) rs67254669
NM_000352.6(ABCC8):c.1572G>A (p.Thr524=) rs61748766
NM_000352.6(ABCC8):c.1643C>T (p.Thr548Met)
NM_000352.6(ABCC8):c.1686C>T (p.His562=) rs1799857
NM_000352.6(ABCC8):c.1707C>T (p.Ala569=) rs147623093
NM_000352.6(ABCC8):c.1926C>G (p.Pro642=) rs75376282
NM_000352.6(ABCC8):c.1947G>A (p.Lys649=) rs1799858
NM_000352.6(ABCC8):c.1958G>A (p.Arg653Gln) rs146378237
NM_000352.6(ABCC8):c.2060C>T (p.Thr687Met) rs150316347
NM_000352.6(ABCC8):c.207T>C (p.Pro69=) rs1048099
NM_000352.6(ABCC8):c.2176G>A (p.Ala726Thr) rs138687850
NM_000352.6(ABCC8):c.2485C>T (p.Leu829=) rs1805036
NM_000352.6(ABCC8):c.2538C>T (p.His846=) rs73423037
NM_000352.6(ABCC8):c.2610C>T (p.Ala870=) rs111967655
NM_000352.6(ABCC8):c.2958G>A (p.Ser986=) rs58820146
NM_000352.6(ABCC8):c.3203C>T (p.Thr1068Met) rs139524121
NM_000352.6(ABCC8):c.330C>T (p.Ala110=) rs8192695
NM_000352.6(ABCC8):c.343A>G (p.Met115Val) rs146695489
NM_000352.6(ABCC8):c.3462C>T (p.Ala1154=)
NM_000352.6(ABCC8):c.354C>T (p.Val118=) rs137873871
NM_000352.6(ABCC8):c.3612C>T (p.Ala1204=) rs149861153
NM_000352.6(ABCC8):c.3650+4C>G
NM_000352.6(ABCC8):c.3819G>A (p.Arg1273=) rs1799859
NM_000352.6(ABCC8):c.3951C>G (p.Leu1317=) rs765708759
NM_000352.6(ABCC8):c.3975C>T (p.Tyr1325=) rs138141427
NM_000352.6(ABCC8):c.3989-10C>T rs373737642
NM_000352.6(ABCC8):c.4008G>C (p.Lys1336Asn) rs67767715
NM_000352.6(ABCC8):c.4077G>A (p.Pro1359=) rs547430068
NM_000352.6(ABCC8):c.4090G>A (p.Val1364Ile) rs138642224
NM_000352.6(ABCC8):c.4105G>T (p.Ala1369Ser) rs757110
NM_000352.6(ABCC8):c.4116G>A (p.Gln1372=) rs562715858
NM_000352.6(ABCC8):c.423G>A (p.Val141=) rs116132921
NM_000352.6(ABCC8):c.4431C>T (p.Gly1477=) rs145673861
NM_000352.6(ABCC8):c.4542C>A (p.Ala1514=) rs113282901
NM_000352.6(ABCC8):c.4647C>T (p.Ile1549=) rs367862706
NM_000352.6(ABCC8):c.4690A>G (p.Lys1564Glu) rs770317560
NM_000352.6(ABCC8):c.486C>T (p.Ile162=) rs149872185
NM_000352.6(ABCC8):c.580-7C>A
NM_000352.6(ABCC8):c.621C>T (p.Pro207=)
NM_000352.6(ABCC8):c.723C>T (p.His241=)
NM_000352.6(ABCC8):c.824G>A (p.Arg275Gln) rs185040406
NM_000352.6(ABCC8):c.853C>T (p.Arg285Trp) rs773087569
NM_001287174.2(ABCC8):c.2041-12C>T rs201419039
NM_001287174.2(ABCC8):c.2117-3C>T rs1799854
NM_001287174.2(ABCC8):c.3402+13G>A rs182340196
NM_001287174.2(ABCC8):c.3561-8C>T rs544550330
NM_001287174.2(ABCC8):c.3870+7G>A rs372198547
NM_001287174.2(ABCC8):c.4122+15C>T rs58368439
NM_001287174.2(ABCC8):c.413-15A>G rs758744263
NM_001287174.2(ABCC8):c.579+14C>T rs2301703

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