Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1159887305
rs1159887305
DNAAF3 ; LOC101930593
G 0.700 CausalMutation CLINVAR

dbSNP: rs116128702
rs116128702
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1164659091
rs1164659091
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs116938457
rs116938457
DNAI1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1175877764
rs1175877764
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1178187217
rs1178187217
DNAH11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs118204041
rs118204041
RSPH4A
T 0.700 CausalMutation CLINVAR

dbSNP: rs118204042
rs118204042
RSPH4A
T 0.700 CausalMutation CLINVAR

dbSNP: rs1188507108
rs1188507108
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1200826286
rs1200826286
DNAAF4 ; DNAAF4-CCPG1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1210953680
rs1210953680
CCDC39
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1212535211
rs1212535211
DNAH11 ; CDCA7L
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121908854
rs121908854
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908855
rs121908855
DNAH11
G 0.700 CausalMutation CLINVAR

dbSNP: rs121918300
rs121918300
NME8 ; EPDR1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1223799853
rs1223799853
DNAH8 ; DNAH8-AS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1233603821
rs1233603821
DNAAF1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1240172375
rs1240172375
DNAI2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1261703349
rs1261703349
DNAH11 ; CDCA7L
T 0.700 CausalMutation CLINVAR

dbSNP: rs1273352530
rs1273352530
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1275367324
rs1275367324
CCDC39
T 0.700 CausalMutation CLINVAR

dbSNP: rs1275718084
rs1275718084
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1283070426
rs1283070426
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1285431486
rs1285431486
CCDC39
T 0.700 CausalMutation CLINVAR

dbSNP: rs1286036654
rs1286036654
DNAH11
T 0.700 CausalMutation CLINVAR