Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77375493
rs77375493
T 0.900 CausalMutation CLINVAR

dbSNP: rs121912472
rs121912472
C 0.810 CausalMutation CLINVAR

dbSNP: rs121913487
rs121913487
0.800 GeneticVariation UNIPROT

dbSNP: rs28931590
rs28931590
A 0.800 CausalMutation CLINVAR

dbSNP: rs121912651
rs121912651
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894360
rs104894360
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502121
rs1060502121
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1169288572
rs1169288572
0.700 GeneticVariation UNIPROT

dbSNP: rs121434637
rs121434637
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912791
rs121912791
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913486
rs121913486
T 0.700 CausalMutation CLINVAR

dbSNP: rs137852728
rs137852728
C 0.700 CausalMutation CLINVAR

dbSNP: rs137852728
rs137852728
CG 0.700 CausalMutation CLINVAR

dbSNP: rs137852730
rs137852730
C 0.700 CausalMutation CLINVAR

dbSNP: rs137852731
rs137852731
TGTAG 0.700 CausalMutation CLINVAR

dbSNP: rs137852732
rs137852732
TCA 0.700 CausalMutation CLINVAR

dbSNP: rs137852733
rs137852733
AG 0.700 CausalMutation CLINVAR

dbSNP: rs1466524306
rs1466524306
0.700 GeneticVariation UNIPROT

dbSNP: rs1554138188
rs1554138188
CTGCA 0.700 CausalMutation CLINVAR

dbSNP: rs1554138188
rs1554138188
CTGCG 0.700 CausalMutation CLINVAR

dbSNP: rs1554138189
rs1554138189
TCTGC 0.700 CausalMutation CLINVAR

dbSNP: rs1555741948
rs1555741948
AGCTGTTCCACCCGCTTGCGCAGGCGGTCATTGTCACTGGTCAGCTCCAGCACCTTCT 0.700 CausalMutation CLINVAR

dbSNP: rs1555741967
rs1555741967
TCAGCTCCAGCACCTTCTGCTGCGTCTC 0.700 CausalMutation CLINVAR

dbSNP: rs1555742213
rs1555742213
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555742295
rs1555742295
CG 0.700 CausalMutation CLINVAR