rs1799937
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1799937(C;C) |
Make rs1799937(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 32389228 |
Gene | WT1 |
is a | snp |
is | mentioned by |
dbSNP | rs1799937 |
dbSNP (classic) | rs1799937 |
ClinGen | rs1799937 |
ebi | rs1799937 |
HLI | rs1799937 |
Exac | rs1799937 |
Gnomad | rs1799937 |
Varsome | rs1799937 |
LitVar | rs1799937 |
Map | rs1799937 |
PheGenI | rs1799937 |
Biobank | rs1799937 |
1000 genomes | rs1799937 |
hgdp | rs1799937 |
ensembl | rs1799937 |
geneview | rs1799937 |
scholar | rs1799937 |
rs1799937 | |
pharmgkb | rs1799937 |
gwascentral | rs1799937 |
openSNP | rs1799937 |
23andMe | rs1799937 |
SNPshot | rs1799937 |
SNPdbe | rs1799937 |
MSV3d | rs1799937 |
GWAS Ctlg | rs1799937 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26573232] A genome-wide association study identifies WT1 variant with better response to 5-fluorouracil, pirarubicin and cyclophosphamide neoadjuvant chemotherapy in breast cancer patients
ClinVar | |
---|---|
Risk | rs1799937(C;C) |
Alt | rs1799937(C;C) |
Reference | Rs1799937(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | WT1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000011.9:g.32410774A>G |
CLNSRC | |
CLNACC | RCV000246241.1, |