Variant (rsID / SNP)
rs1966265
rs1966265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR4. Location: chromosome 5, position 176,516,631. The table records no clinical significance for this variant.
Reference-table entries
FGFR4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:176516631
- HGVS
- NM_001354984.2,c.28G>A,p.Val10Ile
- Allele change
- Missense_V10I
Associated conditions / phenotypes
Diarrhea|Irritable Bowel Syndrome|Constipation|Cervical Cancer|Squamous Cell Carcinoma|Oral Squamous Cell Carcinoma|Colorectal Cancer|Rectum Cancer|Colon Adenocarcinoma|Lung Disease|Bronchopulmonary Dysplasia|Body Mass Index Quantitative Trait Locus 1|Lung Cancer Susceptibility 3|Liver Disease|Adenocarcinoma|Liver Cirrhosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.