rs3763190
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3763190(A;A) |
Make rs3763190(A;G) |
Make rs3763190(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 45379907 |
Gene | RUNX2, SUPT3H |
is a | snp |
is | mentioned by |
dbSNP | rs3763190 |
dbSNP (classic) | rs3763190 |
ClinGen | rs3763190 |
ebi | rs3763190 |
HLI | rs3763190 |
Exac | rs3763190 |
Gnomad | rs3763190 |
Varsome | rs3763190 |
LitVar | rs3763190 |
Map | rs3763190 |
PheGenI | rs3763190 |
Biobank | rs3763190 |
1000 genomes | rs3763190 |
hgdp | rs3763190 |
ensembl | rs3763190 |
geneview | rs3763190 |
scholar | rs3763190 |
rs3763190 | |
pharmgkb | rs3763190 |
gwascentral | rs3763190 |
openSNP | rs3763190 |
23andMe | rs3763190 |
SNPshot | rs3763190 |
SNPdbe | rs3763190 |
MSV3d | rs3763190 |
GWAS Ctlg | rs3763190 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28476574] Association of gene variants of transcription factors PPARγ, RUNX2, Osterix genes and COL2A1, IGFBP3 genes with the development of osteonecrosis of the femoral head in Chinese population.