Variant (rsID / SNP)

rs1127717

rs1127717 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1L1. Location: chromosome 3, position 125,826,059. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALDH1L1Not classified

Variant type: missense_variant
Chromosome / position: 3:125826059
HGVS: NM_001270364.2,c.2408A>G,p.Asp803Gly
Allele change: Silent

Associated conditions / phenotypes

Lymphoma, Non-Hodgkin, Familial|Hepatocellular Carcinoma|Neural Tube Defects|Lymphoma, Hodgkin, Classic

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.