rs2234581

Orientation

minus

Stabilized

minus

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

Make rs2234581(A;A)

Make rs2234581(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32435180

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs2234581
dbSNP (classic)	rs2234581
ClinGen	rs2234581
ebi	rs2234581
HLI	rs2234581
Exac	rs2234581
Gnomad	rs2234581
Varsome	rs2234581
LitVar	rs2234581
Map	rs2234581
PheGenI	rs2234581
Biobank	rs2234581
1000 genomes	rs2234581
hgdp	rs2234581
ensembl	rs2234581
geneview	rs2234581
scholar	rs2234581
google	rs2234581
pharmgkb	rs2234581
gwascentral	rs2234581
openSNP	rs2234581
23andMe	rs2234581
SNPshot	rs2234581
SNPdbe	rs2234581
MSV3d	rs2234581
GWAS Ctlg	rs2234581

Max Magnitude

0

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

ClinVar
Risk	rs2234581(A;A) rs2234581(G;G)
Alt	rs2234581(A;A) rs2234581(G;G)
Reference	Rs2234581(C;C)
Significance	Probable-non-pathogenic
Disease	Drash syndrome Frasier syndrome Wilms tumor 1 Wilms tumor not specified Meacham syndrome Wilms Tumor Diffuse mesangial sclerosis
Variation	info
Gene	WT1 WT1-AS
CLNDBN	Drash syndrome Frasier syndrome Wilms tumor 1 Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome not specified Meacham syndrome Wilms Tumor Diffuse mesangial sclerosis
Reversed	1
HGVS	NC_000011.9:g.32456726G>T
CLNSRC
CLNACC	RCV000229054.2, RCV000250947.1, RCV000259336.1, RCV000265338.1, RCV000319093.1, RCV000373790.1,