Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121907909
rs121907909
WT1
A 0.700 CausalMutation CLINVAR Genetic screening in adolescents with steroid-resistant nephrotic syndrome. 23515051

2013

dbSNP: rs587776576
rs587776576
WT1
T 0.700 CausalMutation CLINVAR Genetic screening in adolescents with steroid-resistant nephrotic syndrome. 23515051

2013

dbSNP: rs121907909
rs121907909
WT1
A 0.700 CausalMutation CLINVAR Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. 21851196

2011

dbSNP: rs1554939839
rs1554939839
WT1
C 0.700 CausalMutation CLINVAR Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development. 15150775

2004

dbSNP: rs121907909
rs121907909
WT1
A 0.700 CausalMutation CLINVAR Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome. 10571943

1999

dbSNP: rs121907909
rs121907909
WT1
A 0.700 CausalMutation CLINVAR Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. 9108089

1997

dbSNP: rs1423753702
rs1423753702
WT1
A 0.700 CausalMutation CLINVAR Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. 9108089

1997

dbSNP: rs121907906
rs121907906
WT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121907922
rs121907922
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554945232
rs1554945232
WT1
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1554946500
rs1554946500
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554946600
rs1554946600
T 0.700 CausalMutation CLINVAR

dbSNP: rs1565000973
rs1565000973
G 0.700 CausalMutation CLINVAR

dbSNP: rs886041222
rs886041222
A 0.700 CausalMutation CLINVAR