ClinVar Miner

Variants in gene HMGCS2 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: 3
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HGVS dbSNP
NM_005518.3(HMGCS2):c.-11C>T rs2289459
NM_005518.3(HMGCS2):c.1419G>A (p.Lys473=) rs142776952
NM_005518.3(HMGCS2):c.862C>A (p.Arg288=) rs142637231

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