RS642742 KITLG

Trait Chr 12:88905968 snv intergenic variant
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What This Variant Does
"Influences appearance gnxp For the rs642742 SNP (184745.0002), located 326 kb upstream of the KITLG ..."
Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Height T β: 0.006 5E-11 PubMed
Population Frequencies
1kG AFR
10.1%
1kG ALL
60.3%
1kG AMR
24.9%
1kG EAS
77.6%
1kG EUR
80%
1kG SAS
20.6%
Other Variants in KITLG
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