List of variants in gene NLRP12 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.2394G>A (p.Gln798=)	rs4806773	0.85135
NM_144687.4(NLRP12):c.-12C>T	rs4539722	0.44990
NM_144687.4(NLRP12):c.116G>T (p.Gly39Val)	rs34436714	0.22387
NM_144687.4(NLRP12):c.1206C>G (p.Phe402Leu)	rs34971363	0.05162
NM_144687.4(NLRP12):c.289+18C>T	rs116129563	0.03610
NM_144687.4(NLRP12):c.1347C>G (p.Ala449=)	rs111234757	0.02160
NM_144687.4(NLRP12):c.609C>T (p.Asp203=)	rs34854934	0.01168
NM_144687.4(NLRP12):c.2784C>T (p.Ala928=)	rs104895569	0.01141
NM_144687.4(NLRP12):c.2576G>A (p.Arg859Gln)	rs79884502	0.00917
NM_144687.4(NLRP12):c.2927+17G>A	rs111310321	0.00864
NM_144687.4(NLRP12):c.969T>G (p.Leu323=)	rs142063194	0.00814
NM_144687.4(NLRP12):c.956C>G (p.Pro319Arg)	rs35401786	0.00803
NM_144687.4(NLRP12):c.424G>A (p.Asp142Asn)	rs34330210	0.00799
NM_144687.4(NLRP12):c.2755C>T (p.Arg919Trp)	rs61741349	0.00716
NM_144687.4(NLRP12):c.2754G>C (p.Leu918=)	rs61741347	0.00692
NM_144687.4(NLRP12):c.2414+16C>T	rs75073147	0.00604
NM_144687.4(NLRP12):c.960G>A (p.Thr320=)	rs77625808	0.00311
NM_144687.4(NLRP12):c.1437G>A (p.Gln479=)	rs77667763	0.00294
NM_144687.4(NLRP12):c.2927+14A>G	rs199476247	0.00247
NM_144687.4(NLRP12):c.1299A>G (p.Ala433=)	rs73608455	0.00194
NM_144687.4(NLRP12):c.819T>C (p.Pro273=)	rs59749540	0.00191
NM_144687.4(NLRP12):c.1352G>A (p.Arg451His)	rs76085152	0.00188
NM_144687.4(NLRP12):c.3024C>T (p.Asn1008=)	rs140769141	0.00142
NM_144687.4(NLRP12):c.2469C>A (p.Leu823=)	rs12460528
NM_144687.4(NLRP12):c.2469C>T (p.Leu823=)	rs12460528
NM_144687.4(NLRP12):c.2830C>A (p.Arg944=)	rs104895570

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