Variant (rsID / SNP)
rs2270981
rs2270981 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPS2. Location: chromosome 17, position 7,216,540. The table records no clinical significance for this variant.
Reference-table entries
GPS2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:7216540
- HGVS
- NM_004489.5,c.795C>T,p.Phe265Phe
- Allele change
- Synonymous_F265F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.