rs1060501253

Orientation

minus

Stabilized

minus

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

Make rs1060501253(-;-)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

32428031

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs1060501253
dbSNP (classic)	rs1060501253
ClinGen	rs1060501253
ebi	rs1060501253
HLI	rs1060501253
Exac	rs1060501253
Gnomad	rs1060501253
Varsome	rs1060501253
LitVar	rs1060501253
Map	rs1060501253
PheGenI	rs1060501253
Biobank	rs1060501253
1000 genomes	rs1060501253
hgdp	rs1060501253
ensembl	rs1060501253
geneview	rs1060501253
scholar	rs1060501253
google	rs1060501253
pharmgkb	rs1060501253
gwascentral	rs1060501253
openSNP	rs1060501253
23andMe	rs1060501253
SNPshot	rs1060501253
SNPdbe	rs1060501253
MSV3d	rs1060501253
GWAS Ctlg	rs1060501253

Max Magnitude

7.5

aka c.161delC (p.Pro54Argfs)

ClinVar
Risk	rs1060501253(-;-)
Alt	rs1060501253(-;-)
Reference	Rs1060501253(C;C)
Significance	Pathogenic
Disease	Drash syndrome Frasier syndrome Wilms tumor 1
Variation	info
Gene	WT1
CLNDBN	Drash syndrome Frasier syndrome Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32449577delG
CLNSRC
CLNACC	RCV000469904.1,