rs9897850
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9897850(C;C) |
Make rs9897850(C;T) |
Make rs9897850(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 6995799 |
Gene | ALOX12, ALOX12-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs9897850 |
dbSNP (classic) | rs9897850 |
ClinGen | rs9897850 |
ebi | rs9897850 |
HLI | rs9897850 |
Exac | rs9897850 |
Gnomad | rs9897850 |
Varsome | rs9897850 |
LitVar | rs9897850 |
Map | rs9897850 |
PheGenI | rs9897850 |
Biobank | rs9897850 |
1000 genomes | rs9897850 |
hgdp | rs9897850 |
ensembl | rs9897850 |
geneview | rs9897850 |
scholar | rs9897850 |
rs9897850 | |
pharmgkb | rs9897850 |
gwascentral | rs9897850 |
openSNP | rs9897850 |
23andMe | rs9897850 |
SNPshot | rs9897850 |
SNPdbe | rs9897850 |
MSV3d | rs9897850 |
GWAS Ctlg | rs9897850 |
GMAF | 0.4421 |
Max Magnitude | 0 |
[PMID 21104233] Polymorphisms in the ALOX12 gene and osteoporosis
[PMID 30277667] ALOX12 gene polymorphisms and serum selenium status in elderly osteoporotic patients.