Variant (rsID / SNP)
rs184917682
rs184917682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTNR1B. Location: chromosome 11, position 92,715,312. Clinical significance in the table: risk factor.
Reference-table entries
MTNR1BRisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:92715312
- Cytoband
- 11q14.3
- HGVS
- NM_005959.5(MTNR1B):c.923A>C (p.Tyr308Ser)
- Allele change
- Missense_Y308S
Associated conditions / phenotypes
Diabetes mellitus type 2, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.