Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853256
rs878853256
TUBB3
0.800 GeneticVariation UNIPROT Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. 20829227

2010
dbSNP: rs878853257
rs878853257
TUBB3
0.800 GeneticVariation UNIPROT Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. 20829227

2010
dbSNP: rs878853258
rs878853258
TUBB3
0.800 GeneticVariation UNIPROT Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. 20829227

2010
dbSNP: rs747480526
rs747480526
TUBB3
T 0.800 CausalMutation CLINVAR

dbSNP: rs747480526
rs747480526
TUBB3
0.800 GeneticVariation UNIPROT

dbSNP: rs878853256
rs878853256
TUBB3
G 0.800 CausalMutation CLINVAR

dbSNP: rs878853257
rs878853257
TUBB3
A 0.800 CausalMutation CLINVAR

dbSNP: rs878853258
rs878853258
TUBB3
T 0.800 CausalMutation CLINVAR

dbSNP: rs1555625363
rs1555625363
TUBB3
T 0.700 GeneticVariation CLINVAR Comprehensive genomic analysis of patients with disorders of cerebral cortical development. 29706646

2018
dbSNP: rs1057518686
rs1057518686
TUBB3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057521924
rs1057521924
TUBB3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267607165
rs267607165
TUBB3
A 0.700 CausalMutation CLINVAR

dbSNP: rs587784505
rs587784505
TUBB3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs878853279
rs878853279
TUBB3
G 0.700 CausalMutation CLINVAR