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Variant (rsID / SNP)

rs4881396

AKR1C3

rs4881396 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKR1C3. Location: chromosome 10, position 5,120,157. The table records no clinical significance for this variant.

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Reference-table entries

AKR1C3Not classified
Variant type
intron_variant
Chromosome / position
10:5120157
HGVS
NM_001253908.2,c.85-18445G>T
Allele change
Silent

Public references

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