rs121907900

Orientation

minus

Stabilized

minus

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

Make rs121907900(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392020

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907900
dbSNP (classic)	rs121907900
ClinGen	rs121907900
ebi	rs121907900
HLI	rs121907900
Exac	rs121907900
Gnomad	rs121907900
Varsome	rs121907900
LitVar	rs121907900
Map	rs121907900
PheGenI	rs121907900
Biobank	rs121907900
1000 genomes	rs121907900
hgdp	rs121907900
ensembl	rs121907900
geneview	rs121907900
scholar	rs121907900
google	rs121907900
pharmgkb	rs121907900
gwascentral	rs121907900
openSNP	rs121907900
23andMe	rs121907900
SNPshot	rs121907900
SNPdbe	rs121907900
MSV3d	rs121907900
GWAS Ctlg	rs121907900

Max Magnitude

7.5

aka c.1384C>T (p.Arg462Trp)

OMIM	607102
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121907900(T;T)
Alt	rs121907900(T;T)
Reference	Rs121907900(C;C)
Significance	Pathogenic
Disease	Drash syndrome Meacham syndrome Diffuse mesangial sclerosis Frasier syndrome Wilms tumor 1 not provided
Variation	info
Gene	WT1
CLNDBN	Drash syndrome Meacham syndrome Diffuse mesangial sclerosis Frasier syndrome Wilms tumor 1 not provided
Reversed	1
HGVS	NC_000011.9:g.32413566G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003656.3, RCV000003657.3, RCV000003658.3, RCV000467701.1, RCV000484426.1,