RS121908146 NLRP3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Hearing loss
autosomal dominant 34
with or without inflammation
Keratitis fugax hereditaria
Chronic infantile neurological
cutaneous and articular syndrome
Autoinflammatory syndrome
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Familial amyloid nephropathy with urticaria AND deafness
Hearing loss
autosomal dominant 34
Other Variants in NLRP3