Variant (rsID / SNP)
rs2123465
rs2123465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIF1. Location: chromosome 2, position 152,320,118. The table records no clinical significance for this variant.
Reference-table entries
RIF1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:152320118
- HGVS
- NM_018151.5,c.4084G>A,p.Val1362Met
- Allele change
- Missense_V1362M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.