Variant (rsID / SNP)
rs2133977
rs2133977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLE3. Location: chromosome 15, position 70,351,788. The table records no clinical significance for this variant.
Reference-table entries
TLE3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:70351788
- HGVS
- NM_005078.4,c.726A>G,p.Gly242Gly
- Allele change
- Synonymous_G235G
Associated conditions / phenotypes
Synonymous_G242G|Synonymous_G242G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.