Variant (rsID / SNP)
rs4717229
rs4717229 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERV3-1. Location: chromosome 7, position 64,451,699. The table records no clinical significance for this variant.
Reference-table entries
ERV3-1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:64451699
- HGVS
- NM_001007253.4,c.1706A>G,p.Asn569Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.