Variant (rsID / SNP)
rs7133698
rs7133698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6C68. Location: chromosome 12, position 55,886,294. The table records no clinical significance for this variant.
Reference-table entries
OR6C68Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:55886294
- HGVS
- NM_001005519.2,c.133G>A,p.Ala45Thr
- Allele change
- Missense_A45T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.