ClinVar Miner

Variants in gene G6PD with conflicting interpretations "other" and "uncertain significance"

Submission 1 (other) minimum review status: Submission 1 (other) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP gnomAD frequency
NM_000402.4(G6PD):c.466A>G (p.Asn156Asp) rs1050829 0.08672
NM_000402.4(G6PD):c.292G>A (p.Val98Met) rs1050828 0.03616
NM_000402.4(G6PD):c.556G>A (p.Glu186Lys) rs137852313 0.00016
NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe) rs137852342 0.00003

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