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
dbSNP: rs2234584
rs2234584
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0027708
Disease:
Nephroblastoma
0.700 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
dbSNP: rs2234584
rs2234584
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0027708
Disease:
Nephroblastoma
0.700 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs2234584
rs2234584
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0027708
Disease:
Nephroblastoma
0.700 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
dbSNP: rs2234584
rs2234584
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0027708
Disease:
Nephroblastoma
0.700 GeneticVariation UNIPROT Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. 15604628 2004