RS145268073 NLRP3
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What This Variant Does
"rs145268073, also known as c.1463G>
Associated Conditions
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Hearing impairment
Autoinflammatory syndrome
NLRP3-related disorder
Keratitis fugax hereditaria
Familial amyloid nephropathy with urticaria AND deafness
Hearing loss
autosomal dominant 34
with or without inflammation
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Hearing impairment
Other Variants in NLRP3