ClinVar Miner

Variants in gene NCF2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP
NM_000433.3(NCF2):c.1001-10T>G rs36113295
NM_000433.3(NCF2):c.1081A>T (p.Thr361Ser) rs147744729
NM_000433.3(NCF2):c.1183C>T (p.Arg395Trp) rs13306575
NM_000433.3(NCF2):c.1256A>T (p.Asn419Ile) rs35012521
NM_000433.3(NCF2):c.1360C>T (p.Pro454Ser) rs55761650
NM_000433.3(NCF2):c.563G>A (p.Arg188Lys) rs115365142

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