Variant (rsID / SNP)
rs1995157
rs1995157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52H1. Location: chromosome 11, position 5,566,051. The table records no clinical significance for this variant.
Reference-table entries
OR52H1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:5566051
- HGVS
- NM_001005289.5,c.685G>T,p.Gly229Cys
- Allele change
- Missense_G235C
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.