ClinVar Miner

List of variants in gene CNNM2 studied for Hypomagnesemia, seizures, and mental retardation 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP
NM_017649.5(CNNM2):c.1069G>A (p.Glu357Lys)	rs786205910
NM_017649.5(CNNM2):c.2240A>G (p.Asn747Ser)	rs988049940
NM_017649.5(CNNM2):c.364G>A (p.Glu122Lys)	rs786205909
NM_017649.5(CNNM2):c.806C>G (p.Ser269Trp)	rs794726858

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