rs16873379
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16873379(C;C) |
Make rs16873379(C;T) |
Make rs16873379(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 45372114 |
Gene | RUNX2, SUPT3H |
is a | snp |
is | mentioned by |
dbSNP | rs16873379 |
dbSNP (classic) | rs16873379 |
ClinGen | rs16873379 |
ebi | rs16873379 |
HLI | rs16873379 |
Exac | rs16873379 |
Gnomad | rs16873379 |
Varsome | rs16873379 |
LitVar | rs16873379 |
Map | rs16873379 |
PheGenI | rs16873379 |
Biobank | rs16873379 |
1000 genomes | rs16873379 |
hgdp | rs16873379 |
ensembl | rs16873379 |
geneview | rs16873379 |
scholar | rs16873379 |
rs16873379 | |
pharmgkb | rs16873379 |
gwascentral | rs16873379 |
openSNP | rs16873379 |
23andMe | rs16873379 |
SNPshot | rs16873379 |
SNPdbe | rs16873379 |
MSV3d | rs16873379 |
GWAS Ctlg | rs16873379 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27704615] Role of Runx2 polymorphisms in risk and prognosis of ossification of posterior longitudinal ligament.