Variant (rsID / SNP)
rs7211875
rs7211875 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TADA2A. Location: chromosome 17, position 35,771,468. The table records no clinical significance for this variant.
Reference-table entries
TADA2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:35771468
- HGVS
- NM_001166105.3,c.16C>T,p.Pro6Ser
- Allele change
- Missense_P6S
Associated conditions / phenotypes
Hepatocellular Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.