RS2074888 TCF3

Health Risk Chr 19:1615796 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Red blood cell distribution width A β: 0.03 7E-12 PubMed
Population Frequencies
gnomAD ALL
97.7%
1kG AFR
97.7%
1kG ALL
11.4%
1kG AMR
10.4%
1kG EAS
37.4%
1kG EUR
98.8%
1kG SAS
92%
Other Variants in TCF3
Ask Dr. Hemsworth about this variant