rs2032502
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2032502(A;A) |
Make rs2032502(A;G) |
Make rs2032502(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 28933788 |
is a | snp |
is | mentioned by |
dbSNP | rs2032502 |
dbSNP (classic) | rs2032502 |
ClinGen | rs2032502 |
ebi | rs2032502 |
HLI | rs2032502 |
Exac | rs2032502 |
Gnomad | rs2032502 |
Varsome | rs2032502 |
LitVar | rs2032502 |
Map | rs2032502 |
PheGenI | rs2032502 |
Biobank | rs2032502 |
1000 genomes | rs2032502 |
hgdp | rs2032502 |
ensembl | rs2032502 |
geneview | rs2032502 |
scholar | rs2032502 |
rs2032502 | |
pharmgkb | rs2032502 |
gwascentral | rs2032502 |
openSNP | rs2032502 |
23andMe | rs2032502 |
SNPshot | rs2032502 |
SNPdbe | rs2032502 |
MSV3d | rs2032502 |
GWAS Ctlg | rs2032502 |
GMAF | 0.1065 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23991122] SNP Association Mapping across the Extended Major Histocompatibility Complex and Risk of B-Cell Precursor Acute Lymphoblastic Leukemia in Children