Variants in gene CLCN1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.2364+10G>A	rs201855153	0.00098
NM_000083.3(CLCN1):c.2834G>T (p.Gly945Val)	rs139659129	0.00091
NM_000083.3(CLCN1):c.501C>G (p.Phe167Leu)	rs149729531	0.00075
NM_000083.3(CLCN1):c.2219C>G (p.Ser740Cys)	rs139262486	0.00031
NM_000083.3(CLCN1):c.314G>A (p.Arg105His)	rs756353660	0.00016
NM_000083.3(CLCN1):c.2722A>G (p.Asn908Asp)	rs146862992	0.00015
NM_000083.3(CLCN1):c.1392C>T (p.Phe464=)	rs201919331	0.00014
NM_000083.3(CLCN1):c.313C>T (p.Arg105Cys)	rs201509501	0.00014
NM_000083.3(CLCN1):c.2230C>A (p.Pro744Thr)	rs149316679	0.00013
NM_000083.3(CLCN1):c.412G>A (p.Val138Ile)	rs762344462	0.00004
NM_000083.3(CLCN1):c.2864A>T (p.Glu955Val)	rs150796358	0.00003
NM_000083.3(CLCN1):c.799C>T (p.Leu267=)	rs1563075864

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