List of variants in gene CLCNKA reported as uncertain significance for Inborn genetic diseases

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004070.4(CLCNKA):c.86G>A (p.Arg29His)	rs760650251	0.00007
NM_004070.4(CLCNKA):c.8A>C (p.Glu3Ala)	rs371201410	0.00001
NM_004070.4(CLCNKA):c.140G>T (p.Gly47Val)	rs545282688
NM_004070.4(CLCNKA):c.221T>A (p.Val74Glu)	rs774646606
NM_004070.4(CLCNKA):c.227G>A (p.Arg76Gln)
NM_004070.4(CLCNKA):c.227G>T (p.Arg76Leu)
NM_004070.4(CLCNKA):c.28G>T (p.Gly10Cys)	rs2524289620
NM_004070.4(CLCNKA):c.80A>T (p.His27Leu)

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