Variant (rsID / SNP)

rs111827785

rs111827785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to G6PD. Clinical significance in the table: Likely benign.

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Reference-table entries

G6PDLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001042351.2(G6PD):c.-111A>G
Allele change: Silent

Associated conditions / phenotypes

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.