Variant (rsID / SNP)

rs201702426

rs201702426 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKR1D1. Location: chromosome 7, position 137,776,608. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

AKR1D1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:137776608
Cytoband: 7q33
HGVS: NM_005989.4(AKR1D1):c.356T>C (p.Ile119Thr)
Allele change: Missense_I119T

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.