List of variants in gene NLRP3 reported as likely benign for perceptual disorders

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met)	rs121908147	0.00835
NM_001243133.2(NLRP3):c.2151-7T>C	rs116546330	0.00084
NM_001243133.2(NLRP3):c.2301C>G (p.Gly767=)	rs150229101	0.00057
NM_001243133.2(NLRP3):c.203T>C (p.Met68Thr)	rs147559626	0.00048
NM_001243133.2(NLRP3):c.1401C>T (p.Leu467=)	rs141637807	0.00029
NM_001243133.2(NLRP3):c.404G>A (p.Arg135His)	rs138946894	0.00029
NM_001243133.2(NLRP3):c.2703T>G (p.Ala901=)	rs138089800	0.00020
NM_001243133.2(NLRP3):c.2611G>A (p.Ala871Thr)	rs201867582	0.00016
NM_001243133.2(NLRP3):c.1623G>A (p.Arg541=)	rs756547568	0.00014
NM_001243133.2(NLRP3):c.1665C>T (p.Asp555=)	rs151097783	0.00007
NM_001243133.2(NLRP3):c.277+11G>A	rs577522959	0.00007
NM_001243133.2(NLRP3):c.2150+16T>C	rs368389907	0.00006
NM_001243133.2(NLRP3):c.2709C>G (p.Ser903=)	rs145787821	0.00006
NM_001243133.2(NLRP3):c.2982G>C (p.Gln994His)	rs148150585	0.00006
NM_001243133.2(NLRP3):c.309T>C (p.Thr103=)	rs199822721	0.00005
NM_001243133.2(NLRP3):c.1625C>T (p.Thr542Met)	rs199856287	0.00004
NM_001243133.2(NLRP3):c.147T>C (p.His49=)	rs199687987	0.00003
NM_001243133.2(NLRP3):c.2321+11G>A	rs371752834	0.00003
NM_001243133.2(NLRP3):c.219C>T (p.Phe73=)	rs201980166	0.00002
NM_001243133.2(NLRP3):c.2738C>T (p.Thr913Met)	rs765925466	0.00002
NM_001243133.2(NLRP3):c.2856G>A (p.Thr952=)	rs200474558	0.00002
NM_001243133.2(NLRP3):c.2058C>T (p.Pro686=)	rs765198709	0.00001
NM_001243133.2(NLRP3):c.2492+13C>T	rs199746830	0.00001
NM_001243133.2(NLRP3):c.369G>A (p.Ser123=)	rs750104265	0.00001
NM_001243133.2(NLRP3):c.1374C>T (p.His458=)	rs180177481
NM_001243133.2(NLRP3):c.1536C>T (p.Cys512=)
NM_001243133.2(NLRP3):c.195G>A (p.Ala65=)	rs201205620
NM_001243133.2(NLRP3):c.2172T>A (p.Thr724=)	rs201102829
NM_001243133.2(NLRP3):c.2185C>A (p.Arg729=)	rs148590318
NM_001243133.2(NLRP3):c.578C>A (p.Thr193Lys)
NM_001243133.2(NLRP3):c.726G>T (p.Ala242=)	rs3806268

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