Variant (rsID / SNP)
rs9639168
rs9639168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETV1. Location: chromosome 7, position 13,978,809. The table records no clinical significance for this variant.
Reference-table entries
ETV1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:13978809
- HGVS
- NM_001370555.1,c.298A>G,p.Ser100Gly
- Allele change
- Silent
Associated conditions / phenotypes
Missense_S82G|Missense_S60G|Missense_S82G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.