ClinVar Miner

Variants in gene CYP7B1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP gnomAD frequency
NM_004820.5(CYP7B1):c.122+19A>T rs7842714 0.39118
NC_000008.11:g.64798895G>C rs117576566 0.02967
NM_004820.5(CYP7B1):c.971G>A (p.Arg324His) rs59035258 0.02701
NM_004820.5(CYP7B1):c.1464G>A (p.Leu488=) rs114797034 0.00140

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