rs6908650
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6908650(A;A) |
Make rs6908650(A;G) |
Make rs6908650(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 45390370 |
Gene | RUNX2 |
is a | snp |
is | mentioned by |
dbSNP | rs6908650 |
dbSNP (classic) | rs6908650 |
ClinGen | rs6908650 |
ebi | rs6908650 |
HLI | rs6908650 |
Exac | rs6908650 |
Gnomad | rs6908650 |
Varsome | rs6908650 |
LitVar | rs6908650 |
Map | rs6908650 |
PheGenI | rs6908650 |
Biobank | rs6908650 |
1000 genomes | rs6908650 |
hgdp | rs6908650 |
ensembl | rs6908650 |
geneview | rs6908650 |
scholar | rs6908650 |
rs6908650 | |
pharmgkb | rs6908650 |
gwascentral | rs6908650 |
openSNP | rs6908650 |
23andMe | rs6908650 |
SNPshot | rs6908650 |
SNPdbe | rs6908650 |
MSV3d | rs6908650 |
GWAS Ctlg | rs6908650 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 27704615] Role of Runx2 polymorphisms in risk and prognosis of ossification of posterior longitudinal ligament.