rs17756311
From SNPedia
Linked to childhood acute lymphoblastic leukemia |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.5 | Possible higher risk of childhood acute lymphoblastic leukemia |
Make rs17756311(A;G) |
Make rs17756311(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 22053896 |
Gene | CDKN2B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs17756311 |
dbSNP (classic) | rs17756311 |
ClinGen | rs17756311 |
ebi | rs17756311 |
HLI | rs17756311 |
Exac | rs17756311 |
Gnomad | rs17756311 |
Varsome | rs17756311 |
LitVar | rs17756311 |
Map | rs17756311 |
PheGenI | rs17756311 |
Biobank | rs17756311 |
1000 genomes | rs17756311 |
hgdp | rs17756311 |
ensembl | rs17756311 |
geneview | rs17756311 |
scholar | rs17756311 |
rs17756311 | |
pharmgkb | rs17756311 |
gwascentral | rs17756311 |
openSNP | rs17756311 |
23andMe | rs17756311 |
SNPshot | rs17756311 |
SNPdbe | rs17756311 |
MSV3d | rs17756311 |
GWAS Ctlg | rs17756311 |
Max Magnitude | 1.5 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23512250] Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.