RS104895097 MEFV

Health Risk Chr 16:3243204 snv missense variant
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What This Variant Does
"rs104895097, also known as c.2282G&gt
Associated Conditions
Familial Mediterranean fever
autosomal dominant
Acute febrile neutrophilic dermatosis
Autoinflammatory syndrome
Inborn genetic diseases
MEFV-related disorder
Familial Mediterranean fever
autosomal dominant
Acute febrile neutrophilic dermatosis
Autoinflammatory syndrome
Inborn genetic diseases
MEFV-related disorder
Population Frequencies
gnomAD ALL
100%
Other Variants in MEFV
rs61752717 rs28940578 rs28940579 rs3743930 rs104895079 rs104895081 rs104895083 rs104895094 rs61732874 rs28940580
Ask Dr. Hemsworth about this variant