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: rs1014959895
rs1014959895
PRMT7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518849
rs1057518849
EHMT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518921
rs1057518921
MED12
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519521
rs1057519521
EBF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692272
rs1131692272
AFF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1135402758
rs1135402758
NUP214
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1135402761
rs1135402761
SYT1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs113871094
rs113871094
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1189909394
rs1189909394
KCNK4 ; KCNK4-TEX40
C 0.700 CausalMutation CLINVAR

dbSNP: rs121434616
rs121434616
CUL4B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1223073957
rs1223073957
MED25
A 0.700 CausalMutation CLINVAR

dbSNP: rs1251713297
rs1251713297
PRMT7
A 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs138632121
rs138632121
HCFC1R1 ; THOC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs142110773
rs142110773
DDC ; FIGNL1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs147030232
rs147030232
BBS2
A 0.700 CausalMutation CLINVAR

dbSNP: rs147484110
rs147484110
CSTB
G 0.700 CausalMutation CLINVAR

dbSNP: rs149830411
rs149830411
KANSL1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553196096
rs1553196096
CDC42
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553196101
rs1553196101
CDC42
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553196134
rs1553196134
CDC42
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553200431
rs1553200431
COL11A1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553511224
rs1553511224
TBR1
TC 0.700 GeneticVariation CLINVAR