Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200482683
rs200482683
NPHS2 ; AXDND1
0.800 GeneticVariation UNIPROT

dbSNP: rs74315345
rs74315345
NPHS2
A 0.800 CausalMutation CLINVAR

dbSNP: rs74315346
rs74315346
NPHS2
C 0.800 CausalMutation CLINVAR

dbSNP: rs74315346
rs74315346
NPHS2
A 0.800 GeneticVariation CLINVAR

dbSNP: rs74315348
rs74315348
NPHS2 ; AXDND1
A 0.800 CausalMutation CLINVAR

dbSNP: rs748812981
rs748812981
NPHS2
0.800 GeneticVariation UNIPROT

dbSNP: rs869025495
rs869025495
NPHS2
0.800 GeneticVariation UNIPROT

dbSNP: rs869025495
rs869025495
NPHS2
A 0.800 CausalMutation CLINVAR

dbSNP: rs1031744496
rs1031744496
NPHS2 ; AXDND1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516395
rs1057516395
NPHS2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516523
rs1057516523
NPHS2 ; AXDND1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516680
rs1057516680
NPHS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516880
rs1057516880
NPHS2
GTA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516900
rs1057516900
NPHS2 ; AXDND1
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517164
rs1057517164
NPHS2 ; AXDND1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499703
rs1060499703
NPHS2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1167223941
rs1167223941
NPHS2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1212702104
rs1212702104
NPHS2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs12568913
rs12568913
NPHS2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1272948499
rs1272948499
NPHS2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1320543506
rs1320543506
NPHS2
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1340195940
rs1340195940
NPHS2
0.700 GeneticVariation UNIPROT

dbSNP: rs1477180313
rs1477180313
NPHS2
0.700 GeneticVariation UNIPROT

dbSNP: rs1553315173
rs1553315173
NPHS2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553316611
rs1553316611
NPHS2
TC 0.700 GeneticVariation CLINVAR