RS61752717 MEFV

Health Risk Chr 16:3243407
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What This Variant Does
"rs61752717, also known as c.2080A&gt
Associated Conditions
Familial Mediterranean fever
autosomal dominant
Acute febrile neutrophilic dermatosis
Autoinflammatory syndrome
Inborn genetic diseases
Recurrent fever
MEFV-related disorder
Familial Mediterranean fever
autosomal dominant
Acute febrile neutrophilic dermatosis
Autoinflammatory syndrome
Inborn genetic diseases
Recurrent fever
MEFV-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Ankylosing spondylitis C OR: 4.76 2E-12 PubMed
Other Variants in MEFV
rs28940578 rs28940579 rs3743930 rs104895079 rs104895081 rs104895083 rs104895094 rs61732874 rs104895097 rs28940580
Ask Dr. Hemsworth about this variant