rs2234593
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2234593(A;A) |
Make rs2234593(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 32392787 |
Gene | WT1 |
is a | snp |
is | mentioned by |
dbSNP | rs2234593 |
dbSNP (classic) | rs2234593 |
ClinGen | rs2234593 |
ebi | rs2234593 |
HLI | rs2234593 |
Exac | rs2234593 |
Gnomad | rs2234593 |
Varsome | rs2234593 |
LitVar | rs2234593 |
Map | rs2234593 |
PheGenI | rs2234593 |
Biobank | rs2234593 |
1000 genomes | rs2234593 |
hgdp | rs2234593 |
ensembl | rs2234593 |
geneview | rs2234593 |
scholar | rs2234593 |
rs2234593 | |
pharmgkb | rs2234593 |
gwascentral | rs2234593 |
openSNP | rs2234593 |
23andMe | rs2234593 |
SNPshot | rs2234593 |
SNPdbe | rs2234593 |
MSV3d | rs2234593 |
GWAS Ctlg | rs2234593 |
Max Magnitude | 0 |
? | (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 not specified |
Variation | info |
Gene | WT1 |
CLNDBN | Drash syndrome not specified |
Reversed | 1 |
HGVS | NC_000011.9:g.32414333G>T |
CLNSRC | |
CLNACC | RCV000210050.1, RCV000253201.1, |