rs121907909

Orientation

minus

Stabilized

minus

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

Make rs121907909(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392032

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907909
dbSNP (classic)	rs121907909
ClinGen	rs121907909
ebi	rs121907909
HLI	rs121907909
Exac	rs121907909
Gnomad	rs121907909
Varsome	rs121907909
LitVar	rs121907909
Map	rs121907909
PheGenI	rs121907909
Biobank	rs121907909
1000 genomes	rs121907909
hgdp	rs121907909
ensembl	rs121907909
geneview	rs121907909
scholar	rs121907909
google	rs121907909
pharmgkb	rs121907909
gwascentral	rs121907909
openSNP	rs121907909
23andMe	rs121907909
SNPshot	rs121907909
SNPdbe	rs121907909
MSV3d	rs121907909
GWAS Ctlg	rs121907909

Max Magnitude

7.5

OMIM	607102
Desc
Variant	0024
Related	also

ClinVar
Risk	rs121907909(T;T)
Alt	rs121907909(T;T)
Reference	Rs121907909(C;C)
Significance	Pathogenic
Disease	Wilms tumor 1 Frasier syndrome Drash syndrome
Variation	info
Gene	WT1
CLNDBN	Wilms tumor 1 Frasier syndrome Drash syndrome
Reversed	1
HGVS	NC_000011.9:g.32413578G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003666.3, RCV000030877.3, RCV000471023.1,