rs78797168
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs78797168(A;A) |
Make rs78797168(A;G) |
Make rs78797168(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 160038159 |
Gene | IGF2R |
is a | snp |
is | mentioned by |
dbSNP | rs78797168 |
dbSNP (classic) | rs78797168 |
ClinGen | rs78797168 |
ebi | rs78797168 |
HLI | rs78797168 |
Exac | rs78797168 |
Gnomad | rs78797168 |
Varsome | rs78797168 |
LitVar | rs78797168 |
Map | rs78797168 |
PheGenI | rs78797168 |
Biobank | rs78797168 |
1000 genomes | rs78797168 |
hgdp | rs78797168 |
ensembl | rs78797168 |
geneview | rs78797168 |
scholar | rs78797168 |
rs78797168 | |
pharmgkb | rs78797168 |
gwascentral | rs78797168 |
openSNP | rs78797168 |
23andMe | rs78797168 |
SNPshot | rs78797168 |
SNPdbe | rs78797168 |
MSV3d | rs78797168 |
GWAS Ctlg | rs78797168 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24024966] |
Trait | Periodontitis (CDC/AAP) |
Title | Genome-wide association study of chronic periodontitis in a general German population. |
Risk Allele | A |
P-val | 2E-6 |
Odds Ratio | 1.75 [1.39-2.22] |