rs2234582

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs2234582(G;T)

Make rs2234582(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32435148

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs2234582
dbSNP (classic)	rs2234582
ClinGen	rs2234582
ebi	rs2234582
HLI	rs2234582
Exac	rs2234582
Gnomad	rs2234582
Varsome	rs2234582
LitVar	rs2234582
Map	rs2234582
PheGenI	rs2234582
Biobank	rs2234582
1000 genomes	rs2234582
hgdp	rs2234582
ensembl	rs2234582
geneview	rs2234582
scholar	rs2234582
google	rs2234582
pharmgkb	rs2234582
gwascentral	rs2234582
openSNP	rs2234582
23andMe	rs2234582
SNPshot	rs2234582
SNPdbe	rs2234582
MSV3d	rs2234582
GWAS Ctlg	rs2234582

GMAF

0.2498

Max Magnitude

0

[PMID 23484026] Single Nucleotide Polymorphisms in the Wilms' Tumour Gene 1 in Clear Cell Renal Cell Carcinoma

ClinVar
Risk	rs2234582(T;T)
Alt	rs2234582(T;T)
Reference	Rs2234582(G;G)
Significance	Non-pathogenic
Disease	not specified Wilms tumor Meacham syndrome Wilms Tumor Diffuse mesangial sclerosis
Variation	info
Gene	WT1 WT1-AS
CLNDBN	not specified Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Meacham syndrome Wilms Tumor Diffuse mesangial sclerosis
Reversed	1
HGVS	NC_000011.9:g.32456694C>A
CLNSRC
CLNACC	RCV000254527.3, RCV000277367.1, RCV000313693.1, RCV000354183.1, RCV000367093.1,