Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556009247
rs1556009247
HDAC8
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1567155145
rs1567155145
PKD1 ; LOC105371049
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567159074
rs1567159074
PKD1 ; LOC105371049
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1567202189
rs1567202189
PKD1
CGTG 0.700 GeneticVariation CLINVAR

dbSNP: rs181208607
rs181208607
PKHD1
T 0.700 CausalMutation CLINVAR

dbSNP: rs386833760
rs386833760
CC2D2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs386834158
rs386834158
CEP290
C 0.700 CausalMutation CLINVAR

dbSNP: rs566014072
rs566014072
PKD1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs747483368
rs747483368
PKD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs751527253
rs751527253
NPHP3 ; NPHP3-ACAD11
C 0.700 CausalMutation CLINVAR

dbSNP: rs754392766
rs754392766
PKHD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs758522600
rs758522600
BBS10
A 0.700 CausalMutation CLINVAR

dbSNP: rs770908659
rs770908659
MKKS
C 0.700 GeneticVariation CLINVAR

dbSNP: rs773386777
rs773386777
CEP290
C 0.700 CausalMutation CLINVAR

dbSNP: rs777269070
rs777269070
PKD1 ; MIR1225 ; LOC105371049
T 0.700 CausalMutation CLINVAR

dbSNP: rs780009030
rs780009030
PKD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs786204707
rs786204707
PKHD1
T 0.700 CausalMutation CLINVAR

dbSNP: rs786205508
rs786205508
MKS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs886039791
rs886039791
TXNDC15
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886039792
rs886039792
TXNDC15
A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039793
rs886039793
MARK4 ; EXOC3L2
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs886039803
rs886039803
MKS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs886039804
rs886039804
TMEM138
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886039805
rs886039805
CEP290
T 0.700 CausalMutation CLINVAR

dbSNP: rs886039806
rs886039806
KIAA0586
G 0.700 GeneticVariation CLINVAR