List of variants in gene NALCN reported as uncertain significance by Genetic Services Laboratory, University 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_052867.4(NALCN):c.1764+6T>G	rs2039697770	0.00001
NM_052867.4(NALCN):c.4745G>A (p.Arg1582His)	rs764045715	0.00001
NM_052867.4(NALCN):c.1631T>C (p.Phe544Ser)	rs2140005193

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