rs28941777

Orientation

minus

Stabilized

minus

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

Make rs28941777(C;C)

Make rs28941777(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392053

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs28941777
dbSNP (classic)	rs28941777
ClinGen	rs28941777
ebi	rs28941777
HLI	rs28941777
Exac	rs28941777
Gnomad	rs28941777
Varsome	rs28941777
LitVar	rs28941777
Map	rs28941777
PheGenI	rs28941777
Biobank	rs28941777
1000 genomes	rs28941777
hgdp	rs28941777
ensembl	rs28941777
geneview	rs28941777
scholar	rs28941777
google	rs28941777
pharmgkb	rs28941777
gwascentral	rs28941777
openSNP	rs28941777
23andMe	rs28941777
SNPshot	rs28941777
SNPdbe	rs28941777
MSV3d	rs28941777
GWAS Ctlg	rs28941777

Max Magnitude

0

OMIM	607102
Desc	MESANGIAL SCLEROSIS, ISOLATED DIFFUSE
Variant	0022
Related	also

ClinVar
Risk	rs28941777(C;C)
Alt	rs28941777(C;C)
Reference	Rs28941777(T;T)
Significance	Pathogenic
Disease	Diffuse mesangial sclerosis
Variation	info
Gene	WT1
CLNDBN	Diffuse mesangial sclerosis
Reversed	1
HGVS	NC_000011.9:g.32413599A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003677.2,