RS104895083 MEFV

Health Risk Chr 16:3247165 snv missense variant
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What This Variant Does
"rs104895083, also known as F479L, is a SNP in the MEFV gene. The equivalent SNP for 23andMe is i4000...
Associated Conditions
Familial Mediterranean fever
Autoinflammatory syndrome
autosomal dominant
Acute febrile neutrophilic dermatosis
Familial Mediterranean fever
Autoinflammatory syndrome
autosomal dominant
Acute febrile neutrophilic dermatosis
Population Frequencies
gnomAD ALL
100%
Other Variants in MEFV
rs61752717 rs28940578 rs28940579 rs3743930 rs104895079 rs104895081 rs104895094 rs61732874 rs104895097 rs28940580
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