Variant (rsID / SNP)
rs7394584
rs7394584 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52N4. Location: chromosome 11, position 5,776,470. The table records no clinical significance for this variant.
Reference-table entries
OR52N4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:5776470
- HGVS
- NM_001005175.5,c.500T>G,p.Leu167Arg
- Allele change
- Missense_L167R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.