ClinVar Miner

List of variants in gene combination ABCC8, LOC110121471 reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_000352.5(ABCC8):c.2475+19G>A rs373894772
NM_000352.6(ABCC8):c.2422C>A (p.Gln808Lys) rs202189540

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