Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918270
rs121918270
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918271
rs121918271
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918272
rs121918272
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918274
rs121918274
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918275
rs121918275
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918276
rs121918276
ROBO3
0.800 GeneticVariation UNIPROT Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004
dbSNP: rs121918270
rs121918270
ROBO3
A 0.800 CausalMutation CLINVAR

dbSNP: rs121918271
rs121918271
ROBO3
C 0.800 CausalMutation CLINVAR

dbSNP: rs121918272
rs121918272
ROBO3
C 0.800 CausalMutation CLINVAR

dbSNP: rs121918274
rs121918274
ROBO3
A 0.800 CausalMutation CLINVAR

dbSNP: rs121918275
rs121918275
ROBO3
C 0.800 CausalMutation CLINVAR

dbSNP: rs121918276
rs121918276
ROBO3
C 0.800 CausalMutation CLINVAR

dbSNP: rs121918273
rs121918273
ROBO3
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918278
rs121918278
ROBO3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1565312182
rs1565312182
ROBO3
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565312616
rs1565312616
ROBO3
A 0.700 CausalMutation CLINVAR

dbSNP: rs775068146
rs775068146
ROBO3
G 0.700 CausalMutation CLINVAR