Variant (rsID / SNP)
rs4804401
rs4804401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7G2. Location: chromosome 19, position 9,213,079. The table records no clinical significance for this variant.
Reference-table entries
OR7G2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:9213079
- HGVS
- NM_001005193.2,c.841T>G,p.Phe281Val
- Allele change
- Missense_F302V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.