Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516005
rs397516005
A 0.760 CausalMutation CLINVAR

dbSNP: rs573916965
rs573916965
A 0.720 CausalMutation CLINVAR

dbSNP: rs1060499604
rs1060499604
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501478
rs1060501478
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060501479
rs1060501479
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1060501480
rs1060501480
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501481
rs1060501481
CTT 0.700 CausalMutation CLINVAR

dbSNP: rs1064792936
rs1064792936
CCTCC 0.700 CausalMutation CLINVAR

dbSNP: rs113276889
rs113276889
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1265248322
rs1265248322
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555120937
rs1555120937
GCCGCCACTTGAGGGAGACCGTGGTGT 0.700 CausalMutation CLINVAR

dbSNP: rs1555121172
rs1555121172
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555122751
rs1555122751
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555122811
rs1555122811
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555123438
rs1555123438
ACCTG 0.700 CausalMutation CLINVAR

dbSNP: rs1555123629
rs1555123629
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555123633
rs1555123633
CATGG 0.700 CausalMutation CLINVAR

dbSNP: rs1565622703
rs1565622703
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1565623216
rs1565623216
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1565625795
rs1565625795
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565628078
rs1565628078
AC 0.700 GeneticVariation CLINVAR

dbSNP: rs1565629792
rs1565629792
C 0.700 CausalMutation CLINVAR

dbSNP: rs1565631381
rs1565631381
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1565631424
rs1565631424
G 0.700 CausalMutation CLINVAR

dbSNP: rs190765116
rs190765116
A 0.700 GeneticVariation CLINVAR