rs587776577

Orientation

plus

Stabilized

minus

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

Make rs587776577(A;A)

Make rs587776577(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32391968

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs587776577
dbSNP (classic)	rs587776577
ClinGen	rs587776577
ebi	rs587776577
HLI	rs587776577
Exac	rs587776577
Gnomad	rs587776577
Varsome	rs587776577
LitVar	rs587776577
Map	rs587776577
PheGenI	rs587776577
Biobank	rs587776577
1000 genomes	rs587776577
hgdp	rs587776577
ensembl	rs587776577
geneview	rs587776577
scholar	rs587776577
google	rs587776577
pharmgkb	rs587776577
gwascentral	rs587776577
openSNP	rs587776577
23andMe	rs587776577
SNPshot	rs587776577
SNPdbe	rs587776577
MSV3d	rs587776577
GWAS Ctlg	rs587776577

Max Magnitude

0

ClinVar
Risk	rs587776577(A;A) Rs587776577(G;G)
Alt	rs587776577(A;A) Rs587776577(G;G)
Reference	Rs587776577(C;C)
Significance	Pathogenic
Disease	Frasier syndrome Diffuse mesangial sclerosis Hereditary nephrotic syndrome not provided
Variation	info
Gene	WT1
CLNDBN	Frasier syndrome Diffuse mesangial sclerosis Hereditary nephrotic syndrome not provided
Reversed	1
HGVS	NC_000011.9:g.32413514G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003674.2, RCV000003675.2, RCV000157584.1, RCV000489749.1,