List of variants in gene CLCN1 reported as uncertain significance by Eurofins Ntd Llc (ga)

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.1392C>T (p.Phe464=)	rs201919331	0.00014
NM_000083.3(CLCN1):c.1222C>G (p.Pro408Ala)	rs202019723	0.00005
NM_000083.3(CLCN1):c.1283T>C (p.Phe428Ser)	rs774843953	0.00003
NM_000083.3(CLCN1):c.568G>A (p.Gly190Arg)	rs369773321
NM_000083.3(CLCN1):c.568_569delinsTC (p.Gly190Ser)	rs797045032

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