List of variants in gene ABCC8 reported as uncertain significance by Molecular Genetics, Madras Diabetes Research Foundation

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.208G>C (p.Gly70Arg)	rs764349043
NM_000352.6(ABCC8):c.2539G>A (p.Ala847Thr)	rs561593131
NM_000352.6(ABCC8):c.2912A>T (p.Glu971Val)	rs1431503235
NM_000352.6(ABCC8):c.2974C>T (p.Arg992Cys)	rs1954577653
NM_000352.6(ABCC8):c.4361T>G (p.Leu1454Arg)	rs2133398519

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