ClinVar Miner

List of variants in gene NLRP12 reported as uncertain significance by Undiagnosed Diseases Network, NIH

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.35G>A (p.Arg12His)	rs376754003	0.00003
NM_144687.4(NLRP12):c.1504_1506del (p.Lys502del)	rs1403147116

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