Variant (rsID / SNP)
rs1801483
rs1801483 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCGR. Location: chromosome 17, position 79,767,715. Clinical significance in the table: Benign.
Reference-table entries
GCGRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:79767715
- Cytoband
- 17q25.3
- HGVS
- NM_000160.5(GCGR):c.118G>A (p.Gly40Ser)
- Allele change
- Missense_G40S
Associated conditions / phenotypes
Type 2 diabetes mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.