rs1839123
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1839123(A;A) |
Make rs1839123(A;G) |
Make rs1839123(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 186678647 |
Gene | ITGAV |
is a | snp |
is | mentioned by |
dbSNP | rs1839123 |
dbSNP (classic) | rs1839123 |
ClinGen | rs1839123 |
ebi | rs1839123 |
HLI | rs1839123 |
Exac | rs1839123 |
Gnomad | rs1839123 |
Varsome | rs1839123 |
LitVar | rs1839123 |
Map | rs1839123 |
PheGenI | rs1839123 |
Biobank | rs1839123 |
1000 genomes | rs1839123 |
hgdp | rs1839123 |
ensembl | rs1839123 |
geneview | rs1839123 |
scholar | rs1839123 |
rs1839123 | |
pharmgkb | rs1839123 |
gwascentral | rs1839123 |
openSNP | rs1839123 |
23andMe | rs1839123 |
SNPshot | rs1839123 |
SNPdbe | rs1839123 |
MSV3d | rs1839123 |
GWAS Ctlg | rs1839123 |
GMAF | 0.2466 |
Max Magnitude | 0 |
[PMID 18694400] Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma
[PMID 26449830] Genetic variants in the ITGB6 gene is associated with the risk of radiation pneumonitis in lung cancer patients treated with thoracic radiation therapy