Variant (rsID / SNP)
rs228648
rs228648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTS2. Location: chromosome 1, position 7,913,430. The table records no clinical significance for this variant.
Reference-table entries
UTS2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:7913430
- HGVS
- NM_021995.2,c.62C>T,p.Thr21Met
- Allele change
- Missense_T21M
Associated conditions / phenotypes
Diabetes Mellitus|Gestational Diabetes|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.