Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122965
rs398122965
TBC1D24
T 0.700 GeneticVariation CLINVAR TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features. 27281533

2016
dbSNP: rs398122965
rs398122965
TBC1D24
T 0.700 GeneticVariation CLINVAR The genetic basis of DOORS syndrome: an exome-sequencing study. 24291220

2014