Variant: rs587776576 

    present in Gene: WT1
    present in Chromosome: 11
    Position on Chromosome: 32391967
    Alleles of this Variant: C/T

rs587776576 in WT1 gene and Denys-Drash Syndrome PMID 9499425 1998 Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

PMID 9398852 1997 Donor splice-site mutations in WT1 are responsible for Frasier syndrome.

PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

PMID 1302008 1992 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.

PMID 10762296 2000 Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

rs587776576 in WT1 gene and Frasier Syndrome PMID 23295293 2012 Frasier syndrome: four new cases with unusual presentations.

PMID 9499425 1998 Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

PMID 28204945 2017 Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.

PMID 1302008 1992 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.

PMID 24856380 2014 Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.

PMID 25818337 2015 Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.

rs587776576 in WT1 gene and NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE PMID 1302008 1992 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.

PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

PMID 20442690 2010 WT1 gene mutations in Chinese children with early onset nephrotic syndrome.

PMID 9499425 1998 Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

rs587776576 in WT1 gene and NEPHROTIC SYNDROME, TYPE 4 PMID 1302008 1992 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.

rs587776576 in WT1 gene and Nephroblastoma PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

rs587776576 in WT1 gene and Steroid-resistant nephrotic syndrome PMID 1302008 1992 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.

rs587776576 in WT1 gene and WAGR Syndrome PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.