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rs2234593

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2234593(A;A)
Make rs2234593(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position32392787
GeneWT1
is asnp
is mentioned by
dbSNPrs2234593
ebirs2234593
HLIrs2234593
Exacrs2234593
Varsomers2234593
Maprs2234593
PheGenIrs2234593
hapmaprs2234593
1000 genomesrs2234593
hgdprs2234593
ensemblrs2234593
gopubmedrs2234593
geneviewrs2234593
scholarrs2234593
googlers2234593
pharmgkbrs2234593
gwascentralrs2234593
openSNPrs2234593
23andMers2234593
23andMe allrs2234593
SNP Nexus

SNPshotrs2234593
SNPdbers2234593
MSV3drs2234593
GWAS Ctlgrs2234593
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 26499507] The Wilms Tumor-1 (WT1) rs2234593 variant is a prognostic factor in normal karyotype acute myeloid leukemia


ClinVar
Risk rs2234593(A;A)
Alt rs2234593(A;A)
Reference rs2234593(C;C)
Significance Non-pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32414333G>T
CLNSRC
CLNACC RCV000210050.1,