rs2017309
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2017309(A;A) |
Make rs2017309(A;T) |
Make rs2017309(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 28735438 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs2017309 |
dbSNP (classic) | rs2017309 |
ClinGen | rs2017309 |
ebi | rs2017309 |
HLI | rs2017309 |
Exac | rs2017309 |
Gnomad | rs2017309 |
Varsome | rs2017309 |
LitVar | rs2017309 |
Map | rs2017309 |
PheGenI | rs2017309 |
Biobank | rs2017309 |
1000 genomes | rs2017309 |
hgdp | rs2017309 |
ensembl | rs2017309 |
geneview | rs2017309 |
scholar | rs2017309 |
rs2017309 | |
pharmgkb | rs2017309 |
gwascentral | rs2017309 |
openSNP | rs2017309 |
23andMe | rs2017309 |
SNPshot | rs2017309 |
SNPdbe | rs2017309 |
MSV3d | rs2017309 |
GWAS Ctlg | rs2017309 |
GMAF | 0.2851 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 17016233] Variant of the CHEK2 gene as a prognostic marker in glioblastoma multiforme.