Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167705
rs1114167705
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1114167706
rs1114167706
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1114167707
rs1114167707
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167708
rs1114167708
CAGTGG 0.700 CausalMutation CLINVAR

dbSNP: rs1114167709
rs1114167709
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167712
rs1114167712
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1114167714
rs1114167714
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167715
rs1114167715
AGC 0.700 CausalMutation CLINVAR

dbSNP: rs1114167717
rs1114167717
CGCTA 0.700 CausalMutation CLINVAR

dbSNP: rs1114167718
rs1114167718
GGAA 0.700 CausalMutation CLINVAR

dbSNP: rs1114167720
rs1114167720
GGAGACTA 0.700 CausalMutation CLINVAR

dbSNP: rs1114167721
rs1114167721
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167723
rs1114167723
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167724
rs1114167724
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167725
rs1114167725
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167728
rs1114167728
G 0.700 CausalMutation CLINVAR

dbSNP: rs1114167729
rs1114167729
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167731
rs1114167731
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167733
rs1114167733
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167740
rs1114167740
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1114167747
rs1114167747
G 0.700 CausalMutation CLINVAR

dbSNP: rs1114167748
rs1114167748
TTCG 0.700 CausalMutation CLINVAR

dbSNP: rs1114167749
rs1114167749
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167750
rs1114167750
C 0.700 CausalMutation CLINVAR

dbSNP: rs1114167751
rs1114167751
A 0.700 CausalMutation CLINVAR