Variant (rsID / SNP)
rs3759091
rs3759091 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBMS2. Location: chromosome 12, position 56,956,213. The table records no clinical significance for this variant.
Reference-table entries
RBMS2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:56956213
- HGVS
- NM_002898.4,c.79T>C,p.Leu27Leu
- Allele change
- Synonymous_L27L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.