Variant (rsID / SNP)
rs7144658
rs7144658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXA1. Location: chromosome 14, position 38,061,742. The table records no clinical significance for this variant.
Reference-table entries
FOXA1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:38061742
- HGVS
- NM_004496.5,c.247G>A,p.Ala83Thr
- Allele change
- Missense_A83T
Associated conditions / phenotypes
Gastric Cancer|Esophageal Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.