Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554389088
rs1554389088
CAMK2B
A 0.700 CausalMutation CLINVAR De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. 29100089

2017
dbSNP: rs146539065
rs146539065
SEPSECS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs553522118
rs553522118
TPP1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587778779
rs587778779
CYP27A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs753614067
rs753614067
BEST1 ; LOC107984334
G 0.700 CausalMutation CLINVAR

dbSNP: rs758022116
rs758022116
RALGAPB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs776969714
rs776969714
SEPSECS
GC 0.700 CausalMutation CLINVAR

dbSNP: rs878853322
rs878853322
PPT1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs878853324
rs878853324
PPT1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs878855331
rs878855331
TPP1
G 0.700 GeneticVariation CLINVAR