SH2B3
HGNC:29605 · SaudiVarKB evidence summary derived from retained literature mentions.
4Gene mentions
4Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in SH2B3 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| celiac disease | — | 1 | 1 |
| endometrial cancer | — | 1 | 1 |
| colorectal cancer | — | 1 | 1 |
Linked variants
Variants normalized to SH2B3| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Not specified | — | 0 | 1 |
| Not specified | — | 265 | 1 |
Supporting publications
4 records- 2022Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.American journal of human geneticsPubMed ↗
- 2020Influence of SH2B3, MTHFD1L, GGCX, and ITGB3 Gene Polymorphisms on theVariability on Warfarin Dosage Requirements and Susceptibility to CVD in the Jordanian Population.Journal of personalized medicinePubMed ↗
- 2015Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.Scientific reportsPubMed ↗
- 2015Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients.Disease markersPubMed ↗