rs878962
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs878962(A;A) |
Make rs878962(A;C) |
Make rs878962(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 3178113 |
Gene | TSPAN9 |
is a | snp |
is | mentioned by |
dbSNP | rs878962 |
dbSNP (classic) | rs878962 |
ClinGen | rs878962 |
ebi | rs878962 |
HLI | rs878962 |
Exac | rs878962 |
Gnomad | rs878962 |
Varsome | rs878962 |
LitVar | rs878962 |
Map | rs878962 |
PheGenI | rs878962 |
Biobank | rs878962 |
1000 genomes | rs878962 |
hgdp | rs878962 |
ensembl | rs878962 |
geneview | rs878962 |
scholar | rs878962 |
rs878962 | |
pharmgkb | rs878962 |
gwascentral | rs878962 |
openSNP | rs878962 |
23andMe | rs878962 |
SNPshot | rs878962 |
SNPdbe | rs878962 |
MSV3d | rs878962 |
GWAS Ctlg | rs878962 |
GMAF | 0.4913 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23746317] |
Trait | Temporomandibular joint disorders |
Title | Genome-wide association study of degenerative bony changes of the temporomandibular joint. |
Risk Allele | C |
P-val | 8E-6 |
Odds Ratio | 1.89 [1.43-2.50] |