Variant (rsID / SNP)

rs121908986

rs121908986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH9A1. Location: chromosome 1, position 165,652,256. Clinical significance in the table: Affects.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALDH9A1Other

Clinical significance (as recorded): Affects
Variant type: single nucleotide variant
Chromosome / position: 1:165652256
Cytoband: 1q24.1
HGVS: NM_000696.4(ALDH9A1):c.419G>C (p.Cys140Ser)
Allele change: Missense_C140S

Associated conditions / phenotypes

ALDH9A1*2 POLYMORPHISM

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.