rs10948172
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10948172(A;A) |
Make rs10948172(A;G) |
Make rs10948172(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 44809954 |
Gene | LOC101929770, SUPT3H |
is a | snp |
is | mentioned by |
dbSNP | rs10948172 |
dbSNP (classic) | rs10948172 |
ClinGen | rs10948172 |
ebi | rs10948172 |
HLI | rs10948172 |
Exac | rs10948172 |
Gnomad | rs10948172 |
Varsome | rs10948172 |
LitVar | rs10948172 |
Map | rs10948172 |
PheGenI | rs10948172 |
Biobank | rs10948172 |
1000 genomes | rs10948172 |
hgdp | rs10948172 |
ensembl | rs10948172 |
geneview | rs10948172 |
scholar | rs10948172 |
rs10948172 | |
pharmgkb | rs10948172 |
gwascentral | rs10948172 |
openSNP | rs10948172 |
23andMe | rs10948172 |
SNPshot | rs10948172 |
SNPdbe | rs10948172 |
MSV3d | rs10948172 |
GWAS Ctlg | rs10948172 |
GMAF | 0.2199 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22763110] |
Trait | Osteoarthritis |
Title | Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. |
Risk Allele | G |
P-val | 6E-7 |
Odds Ratio | 1.08 [1.05-1.12] |
[PMID 30010910] Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis risk.