RS117907409 C1S

Health Risk Chr 12:7066588 snv missense variant
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Associated Conditions
Complement component C1s deficiency
Ehlers-Danlos syndrome
periodontal type 2
Complement component C1s deficiency
Ehlers-Danlos syndrome
periodontal type 2
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Stomatin-like protein 1 levels A OR: 1.28 1E-15 PubMed
Population Frequencies
gnomAD ALL
0.5%
Other Variants in C1S
rs2135727106 rs886040974 rs886040975 rs78523176 rs148105120 rs150549869 rs201750214 rs370458245 rs781944012 rs139493862
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