rs140549288
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs140549288(C;C) |
Make rs140549288(C;G) |
Make rs140549288(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 89339709 |
Gene | IFIT3, LOC101926887 |
is a | snp |
is | mentioned by |
dbSNP | rs140549288 |
dbSNP (classic) | rs140549288 |
ClinGen | rs140549288 |
ebi | rs140549288 |
HLI | rs140549288 |
Exac | rs140549288 |
Gnomad | rs140549288 |
Varsome | rs140549288 |
LitVar | rs140549288 |
Map | rs140549288 |
PheGenI | rs140549288 |
Biobank | rs140549288 |
1000 genomes | rs140549288 |
hgdp | rs140549288 |
ensembl | rs140549288 |
geneview | rs140549288 |
scholar | rs140549288 |
rs140549288 | |
pharmgkb | rs140549288 |
gwascentral | rs140549288 |
openSNP | rs140549288 |
23andMe | rs140549288 |
SNPshot | rs140549288 |
SNPdbe | rs140549288 |
MSV3d | rs140549288 |
GWAS Ctlg | rs140549288 |
Max Magnitude | 0 |
[PMID 26917578] Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.