RS35783914 SPECC1L

Health Risk Chr 22:24313452
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Associated Conditions
Teebi hypertelorism syndrome
Inborn genetic diseases
SPECC1L-related disorder
Teebi hypertelorism syndrome
Inborn genetic diseases
SPECC1L-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Gamma glutamyl transferase levels T OR: 0.16 3E-26 PubMed
Other Variants in SPECC1L
rs190313411 rs200870836 rs143004795 rs2040735453 rs199858278 rs1318284690 rs139099983 rs201626909 rs547014400 rs200239876
Ask Dr. Hemsworth about this variant