rs869025561

Orientation

minus

Stabilized

minus

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

Make rs869025561(G;T)

Make rs869025561(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

32392755

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs869025561
dbSNP (classic)	rs869025561
ClinGen	rs869025561
ebi	rs869025561
HLI	rs869025561
Exac	rs869025561
Gnomad	rs869025561
Varsome	rs869025561
LitVar	rs869025561
Map	rs869025561
PheGenI	rs869025561
Biobank	rs869025561
1000 genomes	rs869025561
hgdp	rs869025561
ensembl	rs869025561
geneview	rs869025561
scholar	rs869025561
google	rs869025561
pharmgkb	rs869025561
gwascentral	rs869025561
openSNP	rs869025561
23andMe	rs869025561
SNPshot	rs869025561
SNPdbe	rs869025561
MSV3d	rs869025561
GWAS Ctlg	rs869025561

Max Magnitude

0

ClinVar
Risk	rs869025561(T;T)
Alt	rs869025561(T;T)
Reference	Rs869025561(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary nephrotic syndrome
Variation	info
Gene	WT1
CLNDBN	Hereditary nephrotic syndrome
Reversed	1
HGVS	NC_000011.9:g.32414301C>A
CLNSRC
CLNACC	RCV000208133.1,