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rs5030320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs5030320(A;G)
Make rs5030320(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position32388456
GeneWT1
is asnp
is mentioned by
dbSNPrs5030320
dbSNP (old)rs5030320
ClinGenrs5030320
ebirs5030320
HLIrs5030320
Exacrs5030320
Gnomadrs5030320
Varsomers5030320
Maprs5030320
PheGenIrs5030320
Biobankrs5030320
1000 genomesrs5030320
hgdprs5030320
ensemblrs5030320
gopubmedrs5030320
geneviewrs5030320
scholarrs5030320
googlers5030320
pharmgkbrs5030320
gwascentralrs5030320
openSNPrs5030320
23andMers5030320
23andMe allrs5030320
SNP Nexus

SNPshotrs5030320
SNPdbers5030320
MSV3drs5030320
GWAS Ctlgrs5030320
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 26046002OA-icon.png] 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,