Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894800
rs104894800
EBP
A 0.800 CausalMutation CLINVAR

dbSNP: rs28935174
rs28935174
EBP
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894792
rs104894792
EBP
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894794
rs104894794
EBP
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894798
rs104894798
EBP
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783600
rs587783600
EBP
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783603
rs587783603
EBP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783606
rs587783606
EBP
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783611
rs587783611
EBP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783612
rs587783612
EBP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783617
rs587783617
EBP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs797045545
rs797045545
EBP
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs797045543
rs797045543
EBP
AT 0.700 CausalMutation CLINVAR

dbSNP: rs587783602
rs587783602
EBP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783605
rs587783605
EBP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783609
rs587783609
EBP
C 0.700 CausalMutation CLINVAR

dbSNP: rs587783614
rs587783614
EBP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs797045544
rs797045544
EBP
CGATA 0.700 CausalMutation CLINVAR

dbSNP: rs1569479901
rs1569479901
EBP
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783610
rs587783610
EBP
G 0.700 GeneticVariation CLINVAR

dbSNP: rs587783615
rs587783615
EBP
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783616
rs587783616
EBP
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783618
rs587783618
EBP
G 0.700 GeneticVariation CLINVAR

dbSNP: rs587783619
rs587783619
EBP
G 0.700 GeneticVariation CLINVAR

dbSNP: rs797045542
rs797045542
EBP
GTGC 0.700 GeneticVariation CLINVAR