ClinVar Miner

List of variants in gene CNNM2 reported as likely pathogenic 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_017649.5(CNNM2):c.2384C>T (p.Ser795Leu)	rs1564873187	0.00001
NM_017649.5(CNNM2):c.135_145del (p.Gly46fs)	rs1590243044

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