rs3111754
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3111754(A;A) |
Make rs3111754(A;G) |
Make rs3111754(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 230868988 |
Gene | ITM2C |
is a | snp |
is | mentioned by |
dbSNP | rs3111754 |
dbSNP (classic) | rs3111754 |
ClinGen | rs3111754 |
ebi | rs3111754 |
HLI | rs3111754 |
Exac | rs3111754 |
Gnomad | rs3111754 |
Varsome | rs3111754 |
LitVar | rs3111754 |
Map | rs3111754 |
PheGenI | rs3111754 |
Biobank | rs3111754 |
1000 genomes | rs3111754 |
hgdp | rs3111754 |
ensembl | rs3111754 |
geneview | rs3111754 |
scholar | rs3111754 |
rs3111754 | |
pharmgkb | rs3111754 |
gwascentral | rs3111754 |
openSNP | rs3111754 |
23andMe | rs3111754 |
SNPshot | rs3111754 |
SNPdbe | rs3111754 |
MSV3d | rs3111754 |
GWAS Ctlg | rs3111754 |
GMAF | 0.45 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals