List of variants in gene CLCN4 reported as uncertain significance for Intellectual disability

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001830.4(CLCN4):c.820G>A (p.Gly274Ser)	rs1924398104
NM_001830.4(CLCN4):c.856T>A (p.Phe286Ile)	rs2147179487
NM_001830.4(CLCN4):c.949G>A (p.Val317Ile)	rs1064796023

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