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rs2234581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2234581(A;A)
Make rs2234581(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position32435180
GeneWT1, WT1-AS
is asnp
is mentioned by
dbSNPrs2234581
ebirs2234581
HLIrs2234581
Exacrs2234581
Varsomers2234581
Maprs2234581
PheGenIrs2234581
hapmaprs2234581
1000 genomesrs2234581
hgdprs2234581
ensemblrs2234581
gopubmedrs2234581
geneviewrs2234581
scholarrs2234581
googlers2234581
pharmgkbrs2234581
gwascentralrs2234581
openSNPrs2234581
23andMers2234581
23andMe allrs2234581
SNP Nexus

SNPshotrs2234581
SNPdbers2234581
MSV3drs2234581
GWAS Ctlgrs2234581
Max Magnitude0

[PMID 23484026OA-icon.png] Single Nucleotide Polymorphisms in the Wilms' Tumour Gene 1 in Clear Cell Renal Cell Carcinoma

ClinVar
Risk rs2234581(A,G;A,G)
Alt rs2234581(A,G;A,G)
Reference rs2234581(C;C)
Significance Probable-non-pathogenic
Disease Drash syndrome Frasier syndrome Wilms tumor 1 Wilms tumor
Variation info
Gene WT1 WT1-AS
CLNDBN Drash syndrome Frasier syndrome Wilms tumor 1 Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome
Reversed 1
HGVS NC_000011.9:g.32456726G>T
CLNSRC
CLNACC RCV000229054.1,