List of variants in gene CLCN7 reported as uncertain significance for Increased bone mineral density

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001287.6(CLCN7):c.857G>A (p.Arg286Gln)	rs760956030	0.00004
NM_001287.6(CLCN7):c.2030G>T (p.Gly677Val)	rs2142366157
NM_001287.6(CLCN7):c.689A>G (p.Lys230Arg)	rs2142382909
NM_001287.6(CLCN7):c.698_712dup (p.Ser237_Val238insGlyValIleLeuSer)	rs2142382851

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