rs6746608
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6746608(A;A) |
Make rs6746608(A;G) |
Make rs6746608(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 111135407 |
Gene | BCL2L11 |
is a | snp |
is | mentioned by |
dbSNP | rs6746608 |
dbSNP (classic) | rs6746608 |
ClinGen | rs6746608 |
ebi | rs6746608 |
HLI | rs6746608 |
Exac | rs6746608 |
Gnomad | rs6746608 |
Varsome | rs6746608 |
LitVar | rs6746608 |
Map | rs6746608 |
PheGenI | rs6746608 |
Biobank | rs6746608 |
1000 genomes | rs6746608 |
hgdp | rs6746608 |
ensembl | rs6746608 |
geneview | rs6746608 |
scholar | rs6746608 |
rs6746608 | |
pharmgkb | rs6746608 |
gwascentral | rs6746608 |
openSNP | rs6746608 |
23andMe | rs6746608 |
SNPshot | rs6746608 |
SNPdbe | rs6746608 |
MSV3d | rs6746608 |
GWAS Ctlg | rs6746608 |
GMAF | 0.4541 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20855536] Germline Variation in Apoptosis Pathway Genes and Risk of non-Hodgkin Lymphoma