Variant (rsID / SNP)
rs2235868
rs2235868 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLP1R. Location: chromosome 6, position 39,040,654. The table records no clinical significance for this variant.
Reference-table entries
GLP1RNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:39040654
- HGVS
- NM_002062.5,c.526A>C,p.Arg176Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
