rs11685758
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11685758(C;C) |
Make rs11685758(C;T) |
Make rs11685758(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 186668641 |
Gene | ITGAV |
is a | snp |
is | mentioned by |
dbSNP | rs11685758 |
dbSNP (classic) | rs11685758 |
ClinGen | rs11685758 |
ebi | rs11685758 |
HLI | rs11685758 |
Exac | rs11685758 |
Gnomad | rs11685758 |
Varsome | rs11685758 |
LitVar | rs11685758 |
Map | rs11685758 |
PheGenI | rs11685758 |
Biobank | rs11685758 |
1000 genomes | rs11685758 |
hgdp | rs11685758 |
ensembl | rs11685758 |
geneview | rs11685758 |
scholar | rs11685758 |
rs11685758 | |
pharmgkb | rs11685758 |
gwascentral | rs11685758 |
openSNP | rs11685758 |
23andMe | rs11685758 |
SNPshot | rs11685758 |
SNPdbe | rs11685758 |
MSV3d | rs11685758 |
GWAS Ctlg | rs11685758 |
GMAF | 0.2511 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18694400] Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma