ClinVar Miner

List of variants studied for anemia, nonspherocytic hemolytic, due to G6PD deficiency by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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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.577G>A (p.Gly193Ser) rs137852314

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