rs12185644, None

N. diseases: 1
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
EPILEPSY, CHILDHOOD ABSENCE, 1
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
0.700 GeneticVariation GWASCAT Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. 30531953 2018