rs16894846
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16894846(A;A) |
Make rs16894846(A;G) |
Make rs16894846(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 34101146 |
Gene | GRM4 |
is a | snp |
is | mentioned by |
dbSNP | rs16894846 |
dbSNP (classic) | rs16894846 |
ClinGen | rs16894846 |
ebi | rs16894846 |
HLI | rs16894846 |
Exac | rs16894846 |
Gnomad | rs16894846 |
Varsome | rs16894846 |
LitVar | rs16894846 |
Map | rs16894846 |
PheGenI | rs16894846 |
Biobank | rs16894846 |
1000 genomes | rs16894846 |
hgdp | rs16894846 |
ensembl | rs16894846 |
geneview | rs16894846 |
scholar | rs16894846 |
rs16894846 | |
pharmgkb | rs16894846 |
gwascentral | rs16894846 |
openSNP | rs16894846 |
23andMe | rs16894846 |
SNPshot | rs16894846 |
SNPdbe | rs16894846 |
MSV3d | rs16894846 |
GWAS Ctlg | rs16894846 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29500710] Genome-wide genotype-based risk model for survival in core binding factor acute myeloid leukemia patients.