Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565000973
rs1565000973
WT1 ; WT1-AS
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565001383
rs1565001383
WT1 ; WT1-AS
A 0.700 CausalMutation CLINVAR

dbSNP: rs28941778
rs28941778
WT1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs28941778
rs28941778
WT1
T 0.700 CausalMutation CLINVAR

dbSNP: rs28942089
rs28942089
WT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs772590420
rs772590420
WT1
0.010 GeneticVariation BEFREE We examined three DDS associated mutations in ZF2 of human WT1 where the normal glutamine at position 369 is replaced by arginine (Q369R), lysine (Q369K) or histidine (Q369H). 27596598

2016
dbSNP: rs1414739809
rs1414739809
PKD1
0.010 GeneticVariation BEFREE Genetic analysis revealed a de novo heterozygous missense mutation c.1186G>A (p.Asp396Asn) in the WT1 gene, confirming the diagnosis of DDS. 24379226

2014
dbSNP: rs760336723
rs760336723
PODXL
0.010 GeneticVariation BEFREE The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome. 15509792

2004