Variant (rsID / SNP)
rs2254174
rs2254174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBATA. Location: chromosome 10, position 72,535,007. The table records no clinical significance for this variant.
Reference-table entries
TBATANot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:72535007
- HGVS
- NM_001318241.2,c.713G>A,p.Arg238Gln
- Allele change
- Silent
Associated conditions / phenotypes
Missense_R237Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.