ClinVar Miner

Variants in gene KCNQ1 with conflicting interpretations "likely benign" and "pathogenic"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (pathogenic) minimum review status: Submission 2 (pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_000218.3(KCNQ1):c.535G>A (p.Gly179Ser) rs199473394 0.00001

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