rs587776576

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;G)	7.5	Wilms tumor susceptibility (predicted)
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587776576(C;T)

Make rs587776576(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32391967

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs587776576
dbSNP (classic)	rs587776576
ClinGen	rs587776576
ebi	rs587776576
HLI	rs587776576
Exac	rs587776576
Gnomad	rs587776576
Varsome	rs587776576
LitVar	rs587776576
Map	rs587776576
PheGenI	rs587776576
Biobank	rs587776576
1000 genomes	rs587776576
hgdp	rs587776576
ensembl	rs587776576
geneview	rs587776576
scholar	rs587776576
google	rs587776576
pharmgkb	rs587776576
gwascentral	rs587776576
openSNP	rs587776576
23andMe	rs587776576
SNPshot	rs587776576
SNPdbe	rs587776576
MSV3d	rs587776576
GWAS Ctlg	rs587776576

Max Magnitude

7.5

ClinVar
Risk	Rs587776576(C;C) rs587776576(T;T)
Alt	Rs587776576(C;C) rs587776576(T;T)
Reference	Rs587776576(G;G)
Significance	Pathogenic
Disease	Drash syndrome Frasier syndrome Hereditary nephrotic syndrome
Variation	info
Gene	WT1
CLNDBN	Drash syndrome Frasier syndrome Hereditary nephrotic syndrome
Reversed	1
HGVS	NC_000011.9:g.32413513C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003665.2, RCV000030876.2, RCV000208283.1,