List of variants in gene ABCC8 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 10

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HGVS	dbSNP	gnomAD frequency
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.1858C>T (p.Arg620Cys)	rs58241708	0.00272
NM_000352.6(ABCC8):c.1630+10C>T	rs188075767	0.00098
NM_000352.6(ABCC8):c.3000C>T (p.Cys1000=)	rs192863214	0.00016
NM_000352.6(ABCC8):c.102G>A (p.Val34=)	rs189746511	0.00011
NM_000352.6(ABCC8):c.1818C>T (p.Ser606=)	rs202207978	0.00004
NM_000352.6(ABCC8):c.4677C>T (p.Phe1559=)	rs771106160	0.00004
NM_000352.6(ABCC8):c.2041-12C>T	rs201419039
NM_000352.6(ABCC8):c.2695-20G>A

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