rs5030320

minus

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

Make rs5030320(A;G)

Make rs5030320(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

32388456

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs5030320
dbSNP (classic)	rs5030320
ClinGen	rs5030320
ebi	rs5030320
HLI	rs5030320
Exac	rs5030320
Gnomad	rs5030320
Varsome	rs5030320
LitVar	rs5030320
Map	rs5030320
PheGenI	rs5030320
Biobank	rs5030320
1000 genomes	rs5030320
hgdp	rs5030320
ensembl	rs5030320
geneview	rs5030320
scholar	rs5030320
google	rs5030320
pharmgkb	rs5030320
gwascentral	rs5030320
openSNP	rs5030320
23andMe	rs5030320
SNPshot	rs5030320
SNPdbe	rs5030320
MSV3d	rs5030320
GWAS Ctlg	rs5030320

Max Magnitude

0

?

(A;A) (A;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	rs5030320(G;G)
Alt	rs5030320(G;G)
Reference	Rs5030320(A;A)
Significance	Non-pathogenic
Disease	Meacham syndrome Diffuse mesangial sclerosis Wilms tumor Wilms Tumor
Variation	info
Gene	WT1
CLNDBN	Meacham syndrome Diffuse mesangial sclerosis Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Wilms Tumor
Reversed	1
HGVS	NC_000011.9:g.32410002T>C
CLNSRC
CLNACC	RCV000271209.1, RCV000326216.1, RCV000381092.1, RCV000384194.1,