Variant (rsID / SNP)
rs11208299
rs11208299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXO5. Location: chromosome 1, position 40,980,731. The table records no clinical significance for this variant.
Reference-table entries
EXO5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:40980731
- HGVS
- NM_001346946.2,c.515G>T,p.Gly172Val
- Allele change
- Missense_G172V
Associated conditions / phenotypes
Missense_G172V|Missense_G172V|Missense_G172V|Missense_G172V|Missense_G172V|Missense_G172V|Missense_G172V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.