RS121908147 NLRP3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Cryopyrin associated periodic syndrome
Kidney disorder
Autoinflammatory syndrome
Hearing loss
autosomal dominant 34
with or without inflammation
Keratitis fugax hereditaria
NLRP3-related disorder
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
Other Variants in NLRP3