rs121907911

Orientation

minus

Stabilized

minus

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

Make rs121907911(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32434815

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs121907911
dbSNP (classic)	rs121907911
ClinGen	rs121907911
ebi	rs121907911
HLI	rs121907911
Exac	rs121907911
Gnomad	rs121907911
Varsome	rs121907911
LitVar	rs121907911
Map	rs121907911
PheGenI	rs121907911
Biobank	rs121907911
1000 genomes	rs121907911
hgdp	rs121907911
ensembl	rs121907911
geneview	rs121907911
scholar	rs121907911
google	rs121907911
pharmgkb	rs121907911
gwascentral	rs121907911
openSNP	rs121907911
23andMe	rs121907911
SNPshot	rs121907911
SNPdbe	rs121907911
MSV3d	rs121907911
GWAS Ctlg	rs121907911

Max Magnitude

7.5

aka c.531C>A (p.Tyr177Ter)

OMIM	607102
Desc
Variant	0027
Related	also

ClinVar
Risk	rs121907911(A;A)
Alt	rs121907911(A;A)
Reference	Rs121907911(C;C)
Significance	Pathogenic
Disease	Wilms tumor 1
Variation	info
Gene	WT1 WT1-AS
CLNDBN	Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32456361G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003681.3,