Gene: CNNM2 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794726858
rs794726858
CNNM2 ; LOC107984265
G 0.800 GeneticVariation CLINVAR CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia. 24699222

2014
dbSNP: rs786205909
rs786205909
CNNM2 ; LOC107984265
A 0.800 CausalMutation CLINVAR

dbSNP: rs786205910
rs786205910
CNNM2 ; LOC107984265
A 0.800 CausalMutation CLINVAR

dbSNP: rs794726858
rs794726858
CNNM2 ; LOC107984265
G 0.800 CausalMutation CLINVAR