Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553770577
rs1553770577
UBA5 ; NPHP3-ACAD11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554768245
rs1554768245
SYNE1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555302200
rs1555302200
RPGRIP1
CTT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555350397
rs1555350397
OTX2
CC 0.700 GeneticVariation CLINVAR

dbSNP: rs2723341
rs2723341
NR2E3
C 0.700 CausalMutation CLINVAR

dbSNP: rs28940877
rs28940877
TYR ; LOC107984363
C 0.700 CausalMutation CLINVAR

dbSNP: rs28940881
rs28940881
TYR ; LOC107984363
G 0.700 CausalMutation CLINVAR

dbSNP: rs375817528
rs375817528
CAPN1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs376823382
rs376823382
TYR ; LOC107984363
G 0.700 GeneticVariation CLINVAR

dbSNP: rs794727792
rs794727792
STXBP1
T 0.700 CausalMutation CLINVAR