ClinVar Miner

Variants in gene ENPP1 with conflicting interpretations "benign" and "risk factor"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (risk factor) minimum review status: Submission 2 (risk factor) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP gnomAD frequency
NM_006208.3(ENPP1):c.517A>C (p.Lys173Gln) rs1044498 0.32168
NM_006208.3(ENPP1):c.2101-11del rs397832689

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