Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs120074160
rs120074160
SBDS
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1232880706
rs1232880706
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs137852981
rs137852981
ZEB2
A 0.700 CausalMutation CLINVAR

dbSNP: rs138632121
rs138632121
HCFC1R1 ; THOC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555247672
rs1555247672
MED13L
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556913268
rs1556913268
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556914274
rs1556914274
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569525894
rs1569525894
SLC9A6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs200426926
rs200426926
THOC6 ; BICDL2
A 0.700 CausalMutation CLINVAR

dbSNP: rs28934906
rs28934906
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs724159955
rs724159955
DYRK1A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs748379243
rs748379243
ERCC8
A 0.700 CausalMutation CLINVAR

dbSNP: rs796052505
rs796052505
GABRG2
A 0.700 CausalMutation CLINVAR

dbSNP: rs886041876
rs886041876
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs1556913180
rs1556913180
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556913258
rs1556913258
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556978515
rs1556978515
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557006873
rs1557006873
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1566913974
rs1566913974
FBN1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1567690011
rs1567690011
PRMT7
C 0.700 CausalMutation CLINVAR

dbSNP: rs180177035
rs180177035
BRAF
C 0.700 CausalMutation CLINVAR

dbSNP: rs397507481
rs397507481
BRAF
C 0.700 CausalMutation CLINVAR

dbSNP: rs724159951
rs724159951
DYRK1A
C 0.700 GeneticVariation CLINVAR