Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517661
rs1057517661
Entrez Id: 51083;107984343
Gene Symbol: GAL;LOC107984343
GAL;LOC107984343
CUI: C4225318
Disease:
EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
0.700 GeneticVariation UNIPROT