rs2234583

Orientation

minus

Stabilized

minus

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

Make rs2234583(C;T)

Make rs2234583(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32434752

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs2234583
dbSNP (classic)	rs2234583
ClinGen	rs2234583
ebi	rs2234583
HLI	rs2234583
Exac	rs2234583
Gnomad	rs2234583
Varsome	rs2234583
LitVar	rs2234583
Map	rs2234583
PheGenI	rs2234583
Biobank	rs2234583
1000 genomes	rs2234583
hgdp	rs2234583
ensembl	rs2234583
geneview	rs2234583
scholar	rs2234583
google	rs2234583
pharmgkb	rs2234583
gwascentral	rs2234583
openSNP	rs2234583
23andMe	rs2234583
SNPshot	rs2234583
SNPdbe	rs2234583
MSV3d	rs2234583
GWAS Ctlg	rs2234583

GMAF

0.1157

Max Magnitude

0

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

ClinVar
Risk	rs2234583(G;G) rs2234583(T;T)
Alt	rs2234583(G;G) rs2234583(T;T)
Reference	Rs2234583(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Wilms tumor Wilms Tumor Diffuse mesangial sclerosis Meacham syndrome Drash syndrome Frasier syndrome Wilms tumor 1
Variation	info
Gene	WT1 WT1-AS
CLNDBN	not specified Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Wilms Tumor Diffuse mesangial sclerosis Meacham syndrome Drash syndrome Frasier syndrome Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32456298G>A; NC_000011.9:g.32456298G>C
CLNSRC
CLNACC	RCV000247609.3, RCV000293694.1, RCV000348640.1, RCV000393785.1, RCV000403336.1, RCV000475587.1,