Variant (rsID / SNP)
rs1243647
rs1243647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASE9. Location: chromosome 14, position 21,024,619. The table records no clinical significance for this variant.
Reference-table entries
RNASE9Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:21024619
- HGVS
- NM_001110358.1,c.625T>C,p.Ser209Pro
- Allele change
- Missense_S204P
Associated conditions / phenotypes
Missense_S204P|Missense_S204P|Synonymous_Y220Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.