Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025495
rs869025495
NPHS2
0.010 GeneticVariation BEFREE In this report, the cases of 3 siblings with steroid-resistant nephrotic syndrome who carry NPHS2 mutations (R238S and P118L) are presented. 15264208

2004
dbSNP: rs121907900
rs121907900
WT1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs386833945
rs386833945
NPHS1 ; KIRREL2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs748106387
rs748106387
SMARCAL1
A 0.700 CausalMutation CLINVAR

dbSNP: rs202128397
rs202128397
CRB2
T 0.710 GeneticVariation CLINVAR

dbSNP: rs119473033
rs119473033
SMARCAL1
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776576
rs587776576
WT1
T 0.700 CausalMutation CLINVAR Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. 1302008

1992
dbSNP: rs879255251
rs879255251
CRB2
TGGCGCGGCCCCGGCCC 0.700 GeneticVariation CLINVAR