ClinVar Miner

Variants in gene G6PD with conflicting interpretations "likely pathogenic" and "other"

Submission 1 (likely pathogenic) minimum review status: Submission 1 (likely pathogenic) method:
Submission 2 (other) minimum review status: Submission 2 (other) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe) rs137852342
NM_000402.4(G6PD):c.1406G>C (p.Arg469Pro) rs137852337
NM_000402.4(G6PD):c.583A>G (p.Asn195Asp) rs137852331
NM_000402.4(G6PD):c.727G>T (p.Val243Leu) rs137852326

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