rs76112010
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs76112010(A;A) |
Make rs76112010(A;G) |
Make rs76112010(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 153682710 |
Gene | TLR2 |
is a | snp |
is | mentioned by |
dbSNP | rs76112010 |
dbSNP (classic) | rs76112010 |
ClinGen | rs76112010 |
ebi | rs76112010 |
HLI | rs76112010 |
Exac | rs76112010 |
Gnomad | rs76112010 |
Varsome | rs76112010 |
LitVar | rs76112010 |
Map | rs76112010 |
PheGenI | rs76112010 |
Biobank | rs76112010 |
1000 genomes | rs76112010 |
hgdp | rs76112010 |
ensembl | rs76112010 |
geneview | rs76112010 |
scholar | rs76112010 |
rs76112010 | |
pharmgkb | rs76112010 |
gwascentral | rs76112010 |
openSNP | rs76112010 |
23andMe | rs76112010 |
SNPshot | rs76112010 |
SNPdbe | rs76112010 |
MSV3d | rs76112010 |
GWAS Ctlg | rs76112010 |
Max Magnitude | 0 |
[PMID 29486365] Importance of common TLR2 genetic variants on clinical phenotypes and risk in tuberculosis disease in a Western Chinese population.