RS3822214 KIT

Health Risk Chr 4:54727297 snv missense variant
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Associated Conditions
Gastrointestinal stromal tumor
Hereditary cancer-predisposing syndrome
Gastrointestinal stromal tumor
Hereditary cancer-predisposing syndrome
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Mast/stem cell growth factor receptor Kit levels C OR: 0.32 5E-16 PubMed
Population Frequencies
gnomAD ALL
0%
1kG AFR
94.9%
1kG ALL
6.4%
1kG AMR
94.4%
1kG EAS
5.3%
1kG EUR
92.1%
1kG SAS
91.3%
Other Variants in KIT
rs121913679 rs121913685 rs794726672 rs794726673 rs121913680 rs794726674 rs794726675 rs121913507 rs587776804 rs2475543943
Ask Dr. Hemsworth about this variant