rs2770146
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2770146(A;A) |
Make rs2770146(A;G) |
Make rs2770146(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 117711060 |
Gene | TLR4 |
is a | snp |
is | mentioned by |
dbSNP | rs2770146 |
dbSNP (classic) | rs2770146 |
ClinGen | rs2770146 |
ebi | rs2770146 |
HLI | rs2770146 |
Exac | rs2770146 |
Gnomad | rs2770146 |
Varsome | rs2770146 |
LitVar | rs2770146 |
Map | rs2770146 |
PheGenI | rs2770146 |
Biobank | rs2770146 |
1000 genomes | rs2770146 |
hgdp | rs2770146 |
ensembl | rs2770146 |
geneview | rs2770146 |
scholar | rs2770146 |
rs2770146 | |
pharmgkb | rs2770146 |
gwascentral | rs2770146 |
openSNP | rs2770146 |
23andMe | rs2770146 |
SNPshot | rs2770146 |
SNPdbe | rs2770146 |
MSV3d | rs2770146 |
GWAS Ctlg | rs2770146 |
GMAF | 0.1621 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21857919] Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)