List of variants in gene CNNM4 reported as benign for not provided

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_020184.4(CNNM4):c.1547-155T>C	rs1318597	0.46864
NM_020184.4(CNNM4):c.1681+145G>A	rs7582249	0.46832
NM_020184.4(CNNM4):c.*2120C>T	rs12846	0.28467
NM_020184.4(CNNM4):c.1402+182G>A	rs72809838	0.24760
NM_020184.4(CNNM4):c.*91C>T	rs7581456	0.09387
NM_020184.4(CNNM4):c.*965A>G	rs3731941	0.07582
NM_020184.4(CNNM4):c.1824G>A (p.Pro608=)	rs36121810	0.02408
NM_020184.4(CNNM4):c.1947C>T (p.Ser649=)	rs41286594	0.01520
NM_020184.4(CNNM4):c.399G>A (p.Val133=)	rs34147094	0.00402
NM_020184.4(CNNM4):c.1461C>T (p.Phe487=)	rs147804021	0.00200
NM_020184.4(CNNM4):c.1851+9G>A	rs185433115	0.00071
NM_020184.4(CNNM4):c.1547-16G>A	rs145616864	0.00066
NM_020184.4(CNNM4):c.591C>T (p.Gly197=)	rs35633391	0.00043
NM_020184.4(CNNM4):c.434T>C (p.Met145Thr)	rs148129550	0.00026
NM_020184.4(CNNM4):c.2259C>T (p.Asp753=)	rs187426899	0.00017
NM_020184.4(CNNM4):c.1701C>T (p.Pro567=)	rs569959107	0.00015
NM_020184.4(CNNM4):c.583C>T (p.Leu195=)	rs778531631	0.00003
NM_020184.4(CNNM4):c.756G>C (p.Leu252=)	rs377727962	0.00001
NC_000002.12:g.96760804G>A	rs3806559
NM_020184.4(CNNM4):c.1546+136C>G	rs115538141

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