List of variants in gene NLRC4 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001199138.2(NLRC4):c.2357G>T (p.Gly786Val)	rs149451729	0.00287
NM_001199138.2(NLRC4):c.478G>A (p.Ala160Thr)	rs113631419	0.00077
NM_001199138.2(NLRC4):c.2369T>C (p.Leu790Pro)	rs202095832	0.00020
NM_001199138.2(NLRC4):c.1+4_1+7del	rs749477750

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