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Items: 2

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrX:153762655
GRCh38:
ChrX:154534440
G6PDD181V, D211Vnot provided, Anemia, nonspherocytic hemolytic, due to G6PD deficiencyConflicting interpretations of pathogenicity
(Oct 15, 2021)
criteria provided, conflicting interpretations
2.
GRCh37:
ChrX:153762655
ChrX:153763492
GRCh38:
ChrX:154534440
ChrX:154535277
G6PD, G6PDD181V, D211V, N126D, N156DG6PD SANTAMARIAother
(May 24, 2017)
no assertion criteria provided