rs1237485
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1237485(C;C) |
Make rs1237485(C;T) |
Make rs1237485(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 28926567 |
is a | snp |
is | mentioned by |
dbSNP | rs1237485 |
dbSNP (classic) | rs1237485 |
ClinGen | rs1237485 |
ebi | rs1237485 |
HLI | rs1237485 |
Exac | rs1237485 |
Gnomad | rs1237485 |
Varsome | rs1237485 |
LitVar | rs1237485 |
Map | rs1237485 |
PheGenI | rs1237485 |
Biobank | rs1237485 |
1000 genomes | rs1237485 |
hgdp | rs1237485 |
ensembl | rs1237485 |
geneview | rs1237485 |
scholar | rs1237485 |
rs1237485 | |
pharmgkb | rs1237485 |
gwascentral | rs1237485 |
openSNP | rs1237485 |
23andMe | rs1237485 |
SNPshot | rs1237485 |
SNPdbe | rs1237485 |
MSV3d | rs1237485 |
GWAS Ctlg | rs1237485 |
GMAF | 0.3586 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23991122] SNP Association Mapping across the Extended Major Histocompatibility Complex and Risk of B-Cell Precursor Acute Lymphoblastic Leukemia in Children