List of variants reported as likely benign for Chronic infantile neurological, cutaneous and articular syndrome

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.2301C>G (p.Gly767=)	rs150229101	0.00057
NM_001243133.2(NLRP3):c.2855C>T (p.Thr952Met)	rs139814109	0.00051
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly)	rs147946775	0.00049
NM_001243133.2(NLRP3):c.1245C>T (p.Ile415=)	rs139852370	0.00045
NM_001243133.2(NLRP3):c.1645T>C (p.Leu549=)	rs144469697	0.00038
NM_001243133.2(NLRP3):c.208G>A (p.Val70Met)	rs117287351	0.00031
NM_001243133.2(NLRP3):c.944C>T (p.Pro315Leu)	rs180177462	0.00010
NM_001243133.2(NLRP3):c.1361G>A (p.Gly454Glu)	rs199696688	0.00006
NM_001243133.2(NLRP3):c.476G>T (p.Ser159Ile)	rs374170024	0.00004

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