Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1034327724
rs1034327724
RSPH4A
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060500990
rs1060500990
CCDC114
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501181
rs1060501181
RPGR
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501454
rs1060501454
DNAH5
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501455
rs1060501455
DNAH5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501456
rs1060501456
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501457
rs1060501457
DNAH5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501458
rs1060501458
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501459
rs1060501459
DNAH5
CTA 0.700 CausalMutation CLINVAR

dbSNP: rs1060501464
rs1060501464
DNAH5
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501466
rs1060501466
DNAH5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501467
rs1060501467
DNAH5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501719
rs1060501719
CCDC40
ACCG 0.700 CausalMutation CLINVAR

dbSNP: rs1060501861
rs1060501861
RSPH1
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1060502202
rs1060502202
DNAI2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502829
rs1060502829
DNAAF1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502831
rs1060502831
DNAAF3 ; LOC101930593
GGCGTC 0.700 CausalMutation CLINVAR

dbSNP: rs1060503041
rs1060503041
DNAH11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060503063
rs1060503063
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503064
rs1060503064
DNAH11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060503095
rs1060503095
DNAAF4 ; DNAAF4-CCPG1
AG 0.700 CausalMutation CLINVAR

dbSNP: rs1060503433
rs1060503433
EFTUD2 ; CCDC103 ; FAM187A
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503495
rs1060503495
DNAI1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060503515
rs1060503515
DNAI1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064792947
rs1064792947
RSPH1
A 0.700 CausalMutation CLINVAR