Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs281875324
rs281875324
G 0.800 CausalMutation CLINVAR

dbSNP: rs80338963
rs80338963
A 0.800 CausalMutation CLINVAR

dbSNP: rs1060500733
rs1060500733
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060500734
rs1060500734
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060500739
rs1060500739
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060500742
rs1060500742
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912577
rs121912577
G 0.700 CausalMutation CLINVAR

dbSNP: rs1316902116
rs1316902116
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555685624
rs1555685624
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555686503
rs1555686503
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555686506
rs1555686506
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555686600
rs1555686600
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555686608
rs1555686608
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555686616
rs1555686616
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1555686624
rs1555686624
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555687378
rs1555687378
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555687572
rs1555687572
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568206602
rs1568206602
TC 0.700 CausalMutation CLINVAR

dbSNP: rs377767324
rs377767324
AAT 0.700 CausalMutation CLINVAR

dbSNP: rs377767325
rs377767325
GTGTCTGT 0.700 CausalMutation CLINVAR

dbSNP: rs377767329
rs377767329
A 0.700 CausalMutation CLINVAR

dbSNP: rs377767330
rs377767330
T 0.700 CausalMutation CLINVAR

dbSNP: rs377767331
rs377767331
G 0.700 CausalMutation CLINVAR

dbSNP: rs377767332
rs377767332
T 0.700 CausalMutation CLINVAR

dbSNP: rs377767333
rs377767333
G 0.700 CausalMutation CLINVAR