Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1010184002
rs1010184002
PEX6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518345
rs1057518345
ADNP
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518786
rs1057518786
SYNGAP1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518794
rs1057518794
ARX
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518845
rs1057518845
SOX5 ; LOC105369696
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518879
rs1057518879
PLOD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518928
rs1057518928
SOX5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519429
rs1057519429
CACNA1A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519437
rs1057519437
EBF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519443
rs1057519443
MPP4
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519444
rs1057519444
SYN3
AA 0.700 CausalMutation CLINVAR

dbSNP: rs1057519450
rs1057519450
HEATR4 ; ACOT1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519521
rs1057519521
EBF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519925
rs1057519925
PIK3CA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060505041
rs1060505041
NACC1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1064795559
rs1064795559
MORC2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307451
rs1085307451
DHX30 ; MIR1226
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085307845
rs1085307845
PHIP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691771
rs1131691771
PHIP ; IRAK1BP1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692228
rs1131692228
ACTL6B
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692229
rs1131692229
KIDINS220
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131692272
rs1131692272
AFF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1135401746
rs1135401746
GNB1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1164484724
rs1164484724
MAN1B1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121434341
rs121434341
CHD7
T 0.700 CausalMutation CLINVAR