List of variants in gene ABCC8 reported as uncertain risk allele for Maturity onset diabetes mellitus in young

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.4308-2A>G	rs886041391	0.00002
NM_000352.6(ABCC8):c.2116+2T>C	rs786204676	0.00001
NM_000352.6(ABCC8):c.2202del (p.Ala736fs)	rs1554924035	0.00001
NM_000352.6(ABCC8):c.3868-1G>A	rs766431403	0.00001
NM_000352.6(ABCC8):c.1347_1348del (p.Ile450fs)	rs1554933565
NM_000352.6(ABCC8):c.1634del (p.Phe545fs)	rs1260178539
NM_000352.6(ABCC8):c.2522G>A (p.Arg841Gln)	rs547150342
NM_000352.6(ABCC8):c.2835_2838del (p.Arg946fs)	rs1554913069
NM_000352.6(ABCC8):c.2921-1G>A	rs772682942
NM_000352.6(ABCC8):c.3107G>A (p.Trp1036Ter)	rs755259997
NM_000352.6(ABCC8):c.4109C>T (p.Pro1370Leu)	rs1554905662
NM_000352.6(ABCC8):c.4160_4162del (p.Phe1387del)	rs151344624
NM_000352.6(ABCC8):c.4322del (p.Pro1441fs)	rs758844607
NM_000352.6(ABCC8):c.4353G>A (p.Trp1451Ter)	rs1057516404
NM_000352.6(ABCC8):c.4613G>A (p.Arg1538Gln)	rs1564869850
NM_000352.6(ABCC8):c.683G>A (p.Gly228Asp)	rs863225280
NM_000352.6(ABCC8):c.695G>A (p.Trp232Ter)	rs1564977373
NM_000352.6(ABCC8):c.725del (p.Lys242fs)	rs1957196622

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