rs3911238
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3911238(C;C) |
Make rs3911238(C;G) |
Make rs3911238(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 186605617 |
Gene | ITGAV |
is a | snp |
is | mentioned by |
dbSNP | rs3911238 |
dbSNP (classic) | rs3911238 |
ClinGen | rs3911238 |
ebi | rs3911238 |
HLI | rs3911238 |
Exac | rs3911238 |
Gnomad | rs3911238 |
Varsome | rs3911238 |
LitVar | rs3911238 |
Map | rs3911238 |
PheGenI | rs3911238 |
Biobank | rs3911238 |
1000 genomes | rs3911238 |
hgdp | rs3911238 |
ensembl | rs3911238 |
geneview | rs3911238 |
scholar | rs3911238 |
rs3911238 | |
pharmgkb | rs3911238 |
gwascentral | rs3911238 |
openSNP | rs3911238 |
23andMe | rs3911238 |
SNPshot | rs3911238 |
SNPdbe | rs3911238 |
MSV3d | rs3911238 |
GWAS Ctlg | rs3911238 |
GMAF | 0.3522 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19818132] The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets
[PMID 21116829] A polymorphism in the integrin alphaV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients.