Variant (rsID / SNP)
rs1644731
rs1644731 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RDH8. Location: chromosome 19, position 10,131,999. The table records no clinical significance for this variant.
Reference-table entries
RDH8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:10131999
- HGVS
- NM_015725.4,c.605T>C,p.Met202Thr
- Allele change
- Missense_M222T
Associated conditions / phenotypes
Myopia|Hypertension, Essential
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.