rs202131936
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202131936(C;C) |
Make rs202131936(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 27204929 |
Gene | TEK |
is a | snp |
is | mentioned by |
dbSNP | rs202131936 |
dbSNP (classic) | rs202131936 |
ClinGen | rs202131936 |
ebi | rs202131936 |
HLI | rs202131936 |
Exac | rs202131936 |
Gnomad | rs202131936 |
Varsome | rs202131936 |
LitVar | rs202131936 |
Map | rs202131936 |
PheGenI | rs202131936 |
Biobank | rs202131936 |
1000 genomes | rs202131936 |
hgdp | rs202131936 |
ensembl | rs202131936 |
geneview | rs202131936 |
scholar | rs202131936 |
rs202131936 | |
pharmgkb | rs202131936 |
gwascentral | rs202131936 |
openSNP | rs202131936 |
23andMe | rs202131936 |
SNPshot | rs202131936 |
SNPdbe | rs202131936 |
MSV3d | rs202131936 |
GWAS Ctlg | rs202131936 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202131936(A;A) rs202131936(C;C) rs202131936(T;T) |
Alt | rs202131936(A;A) rs202131936(C;C) rs202131936(T;T) |
Reference | Rs202131936(G;G) |
Significance | Probable-Pathogenic |
Disease | Acute myeloid leukemia |
Variation | info |
Gene | TEK |
CLNDBN | Acute myeloid leukemia |
Reversed | 0 |
HGVS | NC_000009.11:g.27204927G>C |
CLNSRC | |
CLNACC | RCV000424226.1, |