ClinVar Miner

List of variants reported as likely pathogenic for anemia, nonspherocytic hemolytic by Mendelics

Included ClinVar conditions (4):

Anemia, nonspherocytic hemolytic, due to G6PD deficiency
G6PD deficiency; Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Malaria, susceptibility to; Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Syndromic X-linked intellectual disability Najm type; FG syndrome 4; Anemia, nonspherocytic hemolytic, due to G6PD deficiency

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.1366G>A (p.Asp456Asn)	rs782317415	0.00001

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