Variant (rsID / SNP)
rs6460219
rs6460219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERV3-1. Location: chromosome 7, position 64,453,136. The table records no clinical significance for this variant.
Reference-table entries
ERV3-1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:64453136
- HGVS
- NM_001007253.4,c.269C>T,p.Thr90Ile
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.