RS139574075 COLQ

Health Risk Chr 3:15453899
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital myasthenic syndrome 5
Congenital myasthenic syndrome
Congenital myasthenic syndrome 5
Congenital myasthenic syndrome
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Pancreatic cancer — OR: 14.95 2E-7 PubMed
Other Variants in COLQ
rs104893733 rs104893734 rs121908922 rs769982050 rs759911990 rs121908923 rs121908924 rs1384843815 rs104893735 rs747648795
Ask Dr. Hemsworth about this variant