Variant (rsID / SNP)

rs267606836

rs267606836 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to G6PD. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

G6PDOther

Clinical significance (as recorded): no interpretation for the single variant
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001360016.2(G6PD):c.544C>T (p.Arg182Trp)
Allele change: Missense_R182W

Associated conditions / phenotypes

Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.