List of variants in gene CLCN1 reported as benign by Athena Diagnostics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.1402-9C>T	rs2272252	0.43982
NM_000083.3(CLCN1):c.2284+5C>T	rs74824159	0.01735
NM_000083.3(CLCN1):c.2244G>A (p.Leu748=)	rs78085922	0.01719
NM_000083.3(CLCN1):c.352= (p.Gly118=)	rs10282312	0.01651
NM_000083.3(CLCN1):c.1309G>A (p.Ala437Thr)	rs41276054	0.00925
NM_000083.3(CLCN1):c.1797-9C>T	rs41276057	0.00913
NM_000083.3(CLCN1):c.450C>T (p.Tyr150=)	rs56307536	0.00885
NM_000083.3(CLCN1):c.2136T>C (p.Asp712=)	rs73726622	0.00855
NM_000083.3(CLCN1):c.26G>A (p.Arg9His)	rs115379077	0.00775
NM_000083.3(CLCN1):c.302-4C>T	rs113839156	0.00736
NM_000083.3(CLCN1):c.899G>A (p.Arg300Gln)	rs118066140	0.00465
NM_000083.3(CLCN1):c.86A>C (p.His29Pro)	rs146160029	0.00231
NM_000083.3(CLCN1):c.651C>T (p.Val217=)	rs144109732	0.00145
NM_000083.3(CLCN1):c.2207C>T (p.Thr736Ile)	rs139757692	0.00080

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