ClinVar Miner

List of variants in gene NLRP3 studied for Chronic infantile neurological, cutaneous and articular syndrome; Keratitis fugax hereditaria; Familial amyloid nephropathy with urticaria AND deafness; Familial cold urticaria; DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION

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Total variants: 3
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NM_004895.4(NLRP3):c.1064T>C (p.Leu355Pro) rs28937896
NM_004895.4(NLRP3):c.2126C>A (p.Pro709Gln) rs200378519
NM_004895.4(NLRP3):c.2790A>C (p.Lys930Asn) rs876660975

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