Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs112795301
rs112795301
FOXP1
A 0.710 CausalMutation CLINVAR

dbSNP: rs397514627
rs397514627
CAMK2G
G 0.710 GeneticVariation CLINVAR

dbSNP: rs1010184002
rs1010184002
PEX6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1014959895
rs1014959895
PRMT7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518848
rs1057518848
TCF4
CATTG 0.700 CausalMutation CLINVAR

dbSNP: rs1057518934
rs1057518934
HERC2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518950
rs1057518950
TPO
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692231
rs1131692231
CYFIP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692272
rs1131692272
AFF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1135401761
rs1135401761
AHDC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1223073957
rs1223073957
MED25
A 0.700 CausalMutation CLINVAR

dbSNP: rs122445099
rs122445099
ATRX
A 0.700 CausalMutation CLINVAR

dbSNP: rs1251713297
rs1251713297
PRMT7
A 0.700 CausalMutation CLINVAR

dbSNP: rs1325394060
rs1325394060
HUWE1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553655558
rs1553655558
TRIP12
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554691658
rs1554691658
PTCH1
GGGTCCACAACATCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555103652
rs1555103652
GRIN2B
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555321402
rs1555321402
FOXG1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555954284
rs1555954284
DDX3X
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1556024875
rs1556024875
THOC2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556910184
rs1556910184
HUWE1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1556913258
rs1556913258
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556913268
rs1556913268
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556914274
rs1556914274
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556978515
rs1556978515
HUWE1
C 0.700 GeneticVariation CLINVAR