rs121907906

Orientation

minus

Stabilized

minus

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

Make rs121907906(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392717

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907906
dbSNP (classic)	rs121907906
ClinGen	rs121907906
ebi	rs121907906
HLI	rs121907906
Exac	rs121907906
Gnomad	rs121907906
Varsome	rs121907906
LitVar	rs121907906
Map	rs121907906
PheGenI	rs121907906
Biobank	rs121907906
1000 genomes	rs121907906
hgdp	rs121907906
ensembl	rs121907906
geneview	rs121907906
scholar	rs121907906
google	rs121907906
pharmgkb	rs121907906
gwascentral	rs121907906
openSNP	rs121907906
23andMe	rs121907906
SNPshot	rs121907906
SNPdbe	rs121907906
MSV3d	rs121907906
GWAS Ctlg	rs121907906

Max Magnitude

7.5

aka c.1288C>T (p.Arg430Ter)

OMIM	607102
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121907906(T;T)
Alt	rs121907906(T;T)
Reference	Rs121907906(C;C)
Significance	Pathogenic
Disease	Drash syndrome Wilms tumor 1
Variation	info
Gene	WT1
CLNDBN	Drash syndrome Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32414263G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003670.3, RCV000003671.3,