List of variants in gene combination CLCNKA, LOC106501712 reported as uncertain significance for Bartter disease type 4B

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004070.4(CLCNKA):c.1612C>T (p.Arg538Cys)	rs139564196	0.00350
NM_004070.4(CLCNKA):c.935C>T (p.Thr312Ile)	rs138110172	0.00332
NM_004070.4(CLCNKA):c.1147G>T (p.Asp383Tyr)	rs387907405	0.00041
NM_004070.4(CLCNKA):c.1006G>C (p.Ala336Pro)
NM_004070.4(CLCNKA):c.1425_1426del (p.Ala477fs)	rs2524324333
NM_004070.4(CLCNKA):c.1613G>C (p.Arg538Pro)	rs762119830
NM_004070.4(CLCNKA):c.1972G>A (p.Val658Met)	rs753713670

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