List of variants in gene combination CLCNKA, LOC106501712 reported as likely benign by GeneDx

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004070.4(CLCNKA):c.1000C>G (p.Leu334Val)	rs45588635	0.02154
NM_004070.4(CLCNKA):c.655+241C>T	rs10927888	0.01990
NM_004070.4(CLCNKA):c.359-56C>T	rs116036032	0.01231
NM_004070.4(CLCNKA):c.1622+168T>C	rs369253194	0.01074
NM_004070.4(CLCNKA):c.229+210T>G	rs79241444	0.00971
NM_004070.4(CLCNKA):c.2017-34C>T	rs201201124	0.00888
NM_004070.4(CLCNKA):c.1054-8C>T	rs181589868	0.00746
NM_004070.4(CLCNKA):c.777G>A (p.Glu259=)	rs138578392	0.00744
NM_004070.4(CLCNKA):c.1408+113C>T	rs149145058	0.00539
NM_004070.4(CLCNKA):c.310G>A (p.Val104Ile)	rs116627786	0.00316
NM_004070.4(CLCNKA):c.1005C>T (p.Leu335=)	rs143253425	0.00190
NM_004070.4(CLCNKA):c.1982G>A (p.Arg661Gln)	rs140290085

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