RS138946894 NLRP3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cryopyrin associated periodic syndrome
Autoinflammatory syndrome
Familial amyloid nephropathy with urticaria AND deafness
Inborn genetic diseases
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Hearing loss
autosomal dominant 34
with or without inflammation
Keratitis fugax hereditaria
Cleft palate
Cryopyrin associated periodic syndrome
Autoinflammatory syndrome
Familial amyloid nephropathy with urticaria AND deafness
Other Variants in NLRP3