Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777353
rs587777353
PAM16 ; GLIS2
C 0.710 CausalMutation CLINVAR

dbSNP: rs1060499938
rs1060499938
NPHP3 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1210874691
rs1210874691
NPHP4
A 0.700 CausalMutation CLINVAR

dbSNP: rs121907898
rs121907898
NPHP1
T 0.700 CausalMutation CLINVAR

dbSNP: rs121907899
rs121907899
NPHP1
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918244
rs121918244
IQCB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1278679056
rs1278679056
CEP290
A 0.700 CausalMutation CLINVAR

dbSNP: rs1425211517
rs1425211517
INVS
T 0.700 CausalMutation CLINVAR

dbSNP: rs150001738
rs150001738
INVS
T 0.700 CausalMutation CLINVAR

dbSNP: rs150681845
rs150681845
INTU
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553506530
rs1553506530
TTC21B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553773271
rs1553773271
NPHP3 ; NPHP3-ACAD11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554555063
rs1554555063
TMEM67
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555201796
rs1555201796
CEP290
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555205328
rs1555205328
CEP290
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555212150
rs1555212150
CEP290
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1560000875
rs1560000875
NPHP3 ; NPHP3-ACAD11
C 0.700 CausalMutation CLINVAR

dbSNP: rs1560002147
rs1560002147
NPHP3 ; NPHP3-ACAD11
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1560017690
rs1560017690
NPHP3 ; NPHP3-AS1 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1564123602
rs1564123602
INVS
TGACA 0.700 CausalMutation CLINVAR

dbSNP: rs1565329461
rs1565329461
DYNC2H1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565822519
rs1565822519
CEP290
CT 0.700 CausalMutation CLINVAR

dbSNP: rs182135982
rs182135982
NPHP3 ; NPHP3-ACAD11
T 0.700 CausalMutation CLINVAR

dbSNP: rs373909351
rs373909351
IQCB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs387907009
rs387907009
IQCB1
A 0.700 CausalMutation CLINVAR