RS148150585 NLRP3
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Associated Conditions
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Keratitis fugax hereditaria
Familial cold autoinflammatory syndrome 1
Hearing loss
autosomal dominant 34
with or without inflammation
Chronic infantile neurological
cutaneous and articular syndrome
Inborn genetic diseases
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Keratitis fugax hereditaria
Familial cold autoinflammatory syndrome 1
Hearing loss
Other Variants in NLRP3