rs11662168
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11662168(C;C) |
Make rs11662168(C;T) |
Make rs11662168(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 18 |
Position | 32446429 |
Gene | GAREM1 |
is a | snp |
is | mentioned by |
dbSNP | rs11662168 |
dbSNP (classic) | rs11662168 |
ClinGen | rs11662168 |
ebi | rs11662168 |
HLI | rs11662168 |
Exac | rs11662168 |
Gnomad | rs11662168 |
Varsome | rs11662168 |
LitVar | rs11662168 |
Map | rs11662168 |
PheGenI | rs11662168 |
Biobank | rs11662168 |
1000 genomes | rs11662168 |
hgdp | rs11662168 |
ensembl | rs11662168 |
geneview | rs11662168 |
scholar | rs11662168 |
rs11662168 | |
pharmgkb | rs11662168 |
gwascentral | rs11662168 |
openSNP | rs11662168 |
23andMe | rs11662168 |
SNPshot | rs11662168 |
SNPdbe | rs11662168 |
MSV3d | rs11662168 |
GWAS Ctlg | rs11662168 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26363033] Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia