WT1

is a	gene
is	mentioned by
Full name	Wilms tumor 1
EntrezGene	7490
PheGenI	7490
VariationViewer	7490
ClinVar	WT1
GeneCards	WT1
dbSNP	7490
Diseases	WT1
SADR	7490
HugeNav	7490
wikipedia	WT1
google	WT1
gopubmed	WT1
EVS	WT1
HEFalMp	WT1
MyGene2	WT1
23andMe	WT1
UniProt	P19544
Ensembl	ENSG00000184937
OMIM	607102
# SNPs	37

	Max Magnitude	Chromosome position	Summary
rs1057519745	0	32,396,363
rs1060501253	7.5	32,428,031
rs121907900	7.5	32,392,020
rs121907901	0	32,392,704
rs121907902	0	32,392,013
rs121907903	0	32,392,019
rs121907904	0	32,396,313
rs121907905	0	32,392,723
rs121907906	7.5	32,392,717
rs121907907	0	32,392,682
rs121907908	7.5	32,400,025
rs121907909	7.5	32,392,032
rs121907910	0	32,392,705
rs121907911	7.5	32,434,815
rs16754	0	32,396,399
rs1799925	0	32,435,016
rs1799937	0	32,389,228
rs2234581	0	32,435,180
rs2234582	0	32,435,148
rs2234583	0	32,434,752
rs2234593	0	32,392,787
rs28941777	0	32,392,053
rs28941778	9	32,392,014
rs28941779	9	32,392,026
rs28942089	9	32,392,672
rs3930513	0	32,433,981
rs5030141	0	32,434,307
rs5030315	0	32,388,970
rs5030317	0	32,388,791
rs5030320	0	32,388,456
rs587776573	7.5	32,417,633
rs587776574	7.5	32,399,967
rs587776575	0	32,391,966
rs587776576	7.5	32,391,967
rs587776577	0	32,391,968
rs776155094	0	32,435,210
rs869025561	0	32,392,755

The WT1 gene located on chromosome 11 encodes the Wilms tumor protein.Wikipedia

Several dominantly inherited syndromes are associated with de novo germline mutations in and/or deletions of the WT1 gene, including GHR:

• Denys-Drash syndrome
• Frasier syndrome
• Congenital nephrotic syndrome
• Cytogenetically normal acute myeloid leukemia
• Prostate cancer
• WAGR syndrome
• Kidney cancer (Wilms tumor)

A ClinGen Actionability summary is available here and is associated with certain WT1 genotypes.