rs587776574

Orientation

plus

Stabilized

minus

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

Make rs587776574(-;-)

Make rs587776574(-;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32399967

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs587776574
dbSNP (classic)	rs587776574
ClinGen	rs587776574
ebi	rs587776574
HLI	rs587776574
Exac	rs587776574
Gnomad	rs587776574
Varsome	rs587776574
LitVar	rs587776574
Map	rs587776574
PheGenI	rs587776574
Biobank	rs587776574
1000 genomes	rs587776574
hgdp	rs587776574
ensembl	rs587776574
geneview	rs587776574
scholar	rs587776574
google	rs587776574
pharmgkb	rs587776574
gwascentral	rs587776574
openSNP	rs587776574
23andMe	rs587776574
SNPshot	rs587776574
SNPdbe	rs587776574
MSV3d	rs587776574
GWAS Ctlg	rs587776574

Max Magnitude

7.5

aka c.443delG (p.Gly148Valfs)

ClinVar
Risk	Rs587776574(C;C) rs587776574(-;-)
Alt	Rs587776574(C;C) rs587776574(-;-)
Reference	Rs587776574(G;G)
Significance	Pathogenic
Disease	Wilms tumor 1
Variation	info
Gene	WT1
CLNDBN	Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32421513delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003654.2,