List of variants in gene NLRP3 reported as not provided for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.1302C>T (p.Ser434=)	rs34298354	0.08679
NM_001243133.2(NLRP3):c.-460G>A	rs199475727	0.00046
NM_001243133.2(NLRP3):c.398-85C>T	rs199475732	0.00043
NM_001243133.2(NLRP3):c.397+139T>C	rs199475731	0.00038
NM_001243133.2(NLRP3):c.2834+12G>C	rs199475736	0.00026
NM_001243133.2(NLRP3):c.488A>G (p.Asn163Ser)	rs199475733	0.00015
NM_001243133.2(NLRP3):c.2151-126G>A	rs199476223	0.00010
NM_001243133.2(NLRP3):c.3005+129T>C	rs199475737	0.00010
NM_001243133.2(NLRP3):c.2151-109C>A	rs199475734	0.00004
NM_001243133.2(NLRP3):c.278-28G>A	rs199475728	0.00001
NM_001243133.2(NLRP3):c.291A>G (p.Ala97=)	rs199475729	0.00001
NM_001243133.2(NLRP3):c.2493-7A>T	rs199475735
NM_001243133.2(NLRP3):c.3082dup (p.Val1028fs)	rs199475738
NM_001243133.2(NLRP3):c.397+42T>C	rs199475730
NM_001243133.2(NLRP3):c.726G>A (p.Ala242=)	rs3806268

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