Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2292096
rs2292096
Entrez Id: 23271
Gene Symbol: CAMSAP2
CAMSAP2
CUI: C0014544
Disease:
Epilepsy
0.810 GeneticVariation GWASDB Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. 22116939 2012
dbSNP: rs2292096
rs2292096
Entrez Id: 23271
Gene Symbol: CAMSAP2
CAMSAP2
CUI: C0014544
Disease:
Epilepsy
0.810 GeneticVariation GWASCAT Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. 22116939 2012
dbSNP: rs6691977
rs6691977
Entrez Id: 23271
Gene Symbol: CAMSAP2
CAMSAP2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
C 0.700 GeneticVariation GWASCAT Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. 25751624 2015