WT1, WT1 transcription factor, 7490
N. diseases: 446; N. variants: 61
Source: ALL
| Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
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A | 0.700 | CausalMutation | CLINVAR | Genetic screening in adolescents with steroid-resistant nephrotic syndrome. | 23515051 | 2013 | ||||||
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T | 0.700 | CausalMutation | CLINVAR | Genetic screening in adolescents with steroid-resistant nephrotic syndrome. | 23515051 | 2013 | ||||||
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A | 0.700 | CausalMutation | CLINVAR | Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. | 21851196 | 2011 | ||||||
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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 | ||||||
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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 | ||||||
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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 | ||||||
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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 | ||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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TC | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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T | 0.700 | CausalMutation | CLINVAR | |||||||||
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G | 0.700 | CausalMutation | CLINVAR |