Variant (rsID / SNP)
rs1162753
rs1162753 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RUFY2. Location: chromosome 10, position 70,105,560. The table records no clinical significance for this variant.
Reference-table entries
RUFY2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:70105560
- HGVS
- NM_017987.5,c.1891C>T,p.Leu631Leu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.