ClinVar Miner

List of variants reported as likely benign for hypomagnesemia, seizures, and intellectual disability by Molecular Physiology Group, Radboudumc

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_017649.5(CNNM2):c.551A>G (p.Glu184Gly)
NM_017649.5(CNNM2):c.557G>C (p.Ser186Thr)
NM_017649.5(CNNM2):c.778A>T (p.Ile260Phe)

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