RS180177452 NLRP3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Keratitis fugax hereditaria
Hearing loss
autosomal dominant 34
with or without inflammation
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Keratitis fugax hereditaria
Hearing loss
autosomal dominant 34
Other Variants in NLRP3