List of variants in gene NALCN reported as benign by PreventionGenetics, part of Exact Sciences

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_052867.4(NALCN):c.3570T>C (p.Leu1190=)	rs686141	0.74451
NM_052867.4(NALCN):c.2118+9T>C	rs661585	0.50096
NM_052867.4(NALCN):c.4416A>C (p.Ile1472=)	rs1289556	0.45515
NM_052867.4(NALCN):c.3714C>T (p.Thr1238=)	rs17677552	0.28902
NM_052867.4(NALCN):c.4330+18A>G	rs11616341	0.28723
NM_052867.4(NALCN):c.3210C>T (p.Asn1070=)	rs9513851	0.06211
NM_052867.4(NALCN):c.1836A>G (p.Lys612=)	rs17582557	0.03780
NM_052867.4(NALCN):c.2637-10T>G	rs16958350	0.02553
NM_052867.4(NALCN):c.2305C>T (p.His769Tyr)	rs76776920	0.01886
NM_052867.4(NALCN):c.2520C>T (p.Val840=)	rs34513106	0.01366
NM_052867.4(NALCN):c.515+7G>A	rs41281142	0.01052
NM_052867.4(NALCN):c.2192+5C>T	rs41281140	0.00972
NM_052867.4(NALCN):c.2859C>T (p.Phe953=)	rs34033086	0.00816
NM_052867.4(NALCN):c.2241C>T (p.Pro747=)	rs79264337	0.00512
NM_052867.4(NALCN):c.1593C>T (p.Val531=)	rs3916906

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