List of variants in gene ABCC8 reported as benign for not specified

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.4105G>T (p.Ala1369Ser)	rs757110	0.71935
NM_000352.6(ABCC8):c.2820+17A>G	rs2106865	0.62022
NM_000352.6(ABCC8):c.207T>C (p.Pro69=)	rs1048099	0.47531
NM_000352.6(ABCC8):c.579+14C>T	rs2301703	0.46493
NM_000352.6(ABCC8):c.1686C>T (p.His562=)	rs1799857	0.44260
NM_000352.6(ABCC8):c.3819G>A (p.Arg1273=)	rs1799859	0.39734
NM_000352.6(ABCC8):c.2117-3C>T	rs1799854	0.36733
NM_000352.6(ABCC8):c.1947G>A (p.Lys649=)	rs1799858	0.16150
NM_000352.6(ABCC8):c.2485C>T (p.Leu829=)	rs1805036	0.14682
NM_000352.6(ABCC8):c.330C>T (p.Ala110=)	rs8192695	0.06691
NM_000352.6(ABCC8):c.2277C>T (p.Thr759=)	rs1801261	0.02724
NM_000352.6(ABCC8):c.-19A>G	rs193922394	0.01648
NM_000352.6(ABCC8):c.1158C>T (p.Asn386=)	rs60824529	0.01375
NM_000352.6(ABCC8):c.4120-19C>T	rs1800853	0.01325
NM_000352.6(ABCC8):c.3329+6C>T	rs113873225	0.01304
NM_000352.6(ABCC8):c.3612C>T (p.Ala1204=)	rs149861153	0.01269
NM_000352.6(ABCC8):c.2538C>T (p.His846=)	rs73423037	0.01028
NM_000352.6(ABCC8):c.423G>A (p.Val141=)	rs116132921	0.01009
NM_000352.6(ABCC8):c.1572G>A (p.Thr524=)	rs61748766	0.00948
NM_000352.6(ABCC8):c.4542C>A (p.Ala1514=)	rs113282901	0.00497
NM_000352.6(ABCC8):c.354C>T (p.Val118=)	rs137873871	0.00434
NM_000352.4(ABCC8):c.-72G>A	rs541244107	0.00426
NM_000352.6(ABCC8):c.1926C>G (p.Pro642=)	rs75376282	0.00284
NM_000352.6(ABCC8):c.-8G>T	rs200091822	0.00270
NM_000352.6(ABCC8):c.4545+13C>T	rs78338172	0.00212
NM_000352.6(ABCC8):c.822+20C>T	rs181998151	0.00136
NM_000352.6(ABCC8):c.1707C>T (p.Ala569=)	rs147623093	0.00083
NM_000352.4(ABCC8):c.-544G>A	rs184908312	0.00056
NM_000352.6(ABCC8):c.1678G>A (p.Val560Met)	rs4148619	0.00019
NM_000352.6(ABCC8):c.3000C>T (p.Cys1000=)	rs192863214	0.00016
NM_000352.6(ABCC8):c.3989-10C>T	rs373737642	0.00001

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