Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555682265
rs1555682265
DCC
T 0.700 CausalMutation CLINVAR Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456

2017

dbSNP: rs1057519053
rs1057519053
DCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519054
rs1057519054
DCC
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519055
rs1057519055
DCC
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519056
rs1057519056
DCC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519057
rs1057519057
DCC
A 0.700 CausalMutation CLINVAR

dbSNP: rs199651452
rs199651452
DCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs754914260
rs754914260
DCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs775565634
rs775565634
DCC
A 0.700 CausalMutation CLINVAR