List of variants in gene ABCC8, LOC110121471 studied for Diabetes mellitus, transient neonatal, 2; Hyperinsulinemic hypoglycemia, familial, 1; Leucine-induced hypoglycemia; Type 2 diabetes mellitus; Diabetes mellitus, permanent neonatal 3

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2391-17G>T	rs201484528	0.00206
NM_000352.6(ABCC8):c.2390+17G>C	rs200705248	0.00035
NM_000352.6(ABCC8):c.2304C>T (p.Pro768=)	rs199541853	0.00010
NM_000352.6(ABCC8):c.2422C>A (p.Gln808Lys)	rs202189540	0.00006
NM_000352.6(ABCC8):c.2473C>A (p.Arg825=)	rs779736828	0.00002
NM_000352.6(ABCC8):c.2403C>A (p.Val801=)	rs148863748	0.00001
NM_000352.6(ABCC8):c.2305G>A (p.Val769Met)
NM_000352.6(ABCC8):c.2309C>G (p.Ala770Gly)
NM_000352.6(ABCC8):c.2319G>C (p.Ser773=)	rs766321878
NM_000352.6(ABCC8):c.2389C>G (p.Arg797Gly)
NM_000352.6(ABCC8):c.2391-5G>T
NM_000352.6(ABCC8):c.2391-9C>A
NM_000352.6(ABCC8):c.2434G>A (p.Asp812Asn)
NM_000352.6(ABCC8):c.2449G>A (p.Gly817Arg)
NM_000352.6(ABCC8):c.2465T>C (p.Ile822Thr)
NM_000352.6(ABCC8):c.2470G>T (p.Glu824Ter)
NM_000352.6(ABCC8):c.2473C>T (p.Arg825Trp)	rs779736828

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