ClinVar Miner

Variants in gene PROC with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
NM_000312.4(PROC):c.-50A>T rs1799810 0.44475
NM_000312.4(PROC):c.768T>C (p.Asp256=) rs5937 0.27234
NM_000312.4(PROC):c.30C>T (p.Phe10=) rs148490199 0.00059

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