Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514627
rs397514627
0.710 GeneticVariation BEFREE Recently, a de novo candidate mutation (p.Arg292Pro) in the gamma isoform of CAMK2 (CAMK2G) was identified in a patient with severe intellectual disability (ID), but the mechanism(s) by which this mutation causes ID is unknown. 30184290

2018

dbSNP: rs397514627
rs397514627
G 0.710 GeneticVariation CLINVAR