ClinVar Miner

List of variants in gene INSR reported as likely benign for Bailey-Bloch congenital myopathy

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816 0.00500

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