rs2290083
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 0 | common in complete genomics |
Make rs2290083(C;C) |
Make rs2290083(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 186669014 |
Gene | ITGAV |
is a | snp |
is | mentioned by |
dbSNP | rs2290083 |
dbSNP (classic) | rs2290083 |
ClinGen | rs2290083 |
ebi | rs2290083 |
HLI | rs2290083 |
Exac | rs2290083 |
Gnomad | rs2290083 |
Varsome | rs2290083 |
LitVar | rs2290083 |
Map | rs2290083 |
PheGenI | rs2290083 |
Biobank | rs2290083 |
1000 genomes | rs2290083 |
hgdp | rs2290083 |
ensembl | rs2290083 |
geneview | rs2290083 |
scholar | rs2290083 |
rs2290083 | |
pharmgkb | rs2290083 |
gwascentral | rs2290083 |
openSNP | rs2290083 |
23andMe | rs2290083 |
SNPshot | rs2290083 |
SNPdbe | rs2290083 |
MSV3d | rs2290083 |
GWAS Ctlg | rs2290083 |
GMAF | 0.4619 |
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