rs12971396
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12971396(C;C) |
Make rs12971396(C;G) |
Make rs12971396(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 39247226 |
Gene | IFNL3, IFNL4 |
is a | snp |
is | mentioned by |
dbSNP | rs12971396 |
dbSNP (classic) | rs12971396 |
ClinGen | rs12971396 |
ebi | rs12971396 |
HLI | rs12971396 |
Exac | rs12971396 |
Gnomad | rs12971396 |
Varsome | rs12971396 |
LitVar | rs12971396 |
Map | rs12971396 |
PheGenI | rs12971396 |
Biobank | rs12971396 |
1000 genomes | rs12971396 |
hgdp | rs12971396 |
ensembl | rs12971396 |
geneview | rs12971396 |
scholar | rs12971396 |
rs12971396 | |
pharmgkb | rs12971396 |
gwascentral | rs12971396 |
openSNP | rs12971396 |
23andMe | rs12971396 |
SNPshot | rs12971396 |
SNPdbe | rs12971396 |
MSV3d | rs12971396 |
GWAS Ctlg | rs12971396 |
Max Magnitude | 0 |
[PMID 29055988] [Association of HLA-DQ and IFNL4 polymorphisms with hepatitis B virus infection and clearance].