rs7903146
NM_001367943.1(TCF7L2):c.450+33966C>T
- Diabetes mellitus type 2, susceptibility toRisk factor · germline
gnomAD allele frequency 2.56e-1
rs7903146 is a genetic variant located in the TCF7L2 gene. dbsnp · gene
In gnomAD, rs7903146 has an overall allele frequency of 25.6%. gnomad · frequency
In ClinVar, rs7903146 is classified as Risk factor for Diabetes mellitus type 2, susceptibility to (0 review stars, germline; last evaluated 2011-09-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 830f05b87044656f · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0
Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.