Variant (rsID / SNP)

rs1781931

rs1781931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKR1C8, AKR1C8P. Location: chromosome 10, position 5,197,881. The table records no clinical significance for this variant.

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Reference-table entries

AKR1C8Not classified

Variant type: synonymous_variant
Chromosome / position: 10:5197881
HGVS: NM_001395972.1,c.870T>C,p.Asp290Asp
Allele change: Silent

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.