Variant (rsID / SNP)
rs7030820
rs7030820 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR13F1. Location: chromosome 9, position 107,267,304. The table records no clinical significance for this variant.
Reference-table entries
OR13F1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 9:107267304
- HGVS
- NM_001004485.1,c.761C>T,p.Thr254Met
- Allele change
- Missense_T254M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.