Variant (rsID / SNP)

rs2228093

rs2228093 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1B1. Location: chromosome 9, position 38,396,002. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALDH1B1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:38396002
Cytoband: 9p13.1
HGVS: NM_000692.5(ALDH1B1):c.257C>T (p.Ala86Val)
Allele change: Missense_A86V

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.