rs5030317

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs5030317(C;C)

Make rs5030317(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

32388791

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs5030317
dbSNP (classic)	rs5030317
ClinGen	rs5030317
ebi	rs5030317
HLI	rs5030317
Exac	rs5030317
Gnomad	rs5030317
Varsome	rs5030317
LitVar	rs5030317
Map	rs5030317
PheGenI	rs5030317
Biobank	rs5030317
1000 genomes	rs5030317
hgdp	rs5030317
ensembl	rs5030317
geneview	rs5030317
scholar	rs5030317
google	rs5030317
pharmgkb	rs5030317
gwascentral	rs5030317
openSNP	rs5030317
23andMe	rs5030317
SNPshot	rs5030317
SNPdbe	rs5030317
MSV3d	rs5030317
GWAS Ctlg	rs5030317

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

[PMID 26046002 ] Association between WT1 polymorphisms and susceptibility to breast cancer: results from a case-control study in a southwestern Chinese population

ClinVar
Risk	rs5030317(C;C)
Alt	rs5030317(C;C)
Reference	Rs5030317(G;G)
Significance	Non-pathogenic
Disease	Wilms Tumor Wilms tumor Diffuse mesangial sclerosis Meacham syndrome
Variation	info
Gene	WT1
CLNDBN	Wilms Tumor Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Diffuse mesangial sclerosis Meacham syndrome
Reversed	1
HGVS	NC_000011.9:g.32410337C>G
CLNSRC
CLNACC	RCV000286453.1, RCV000290056.1, RCV000320478.1, RCV000377465.1,