rs9896933
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9896933(C;C) |
Make rs9896933(C;T) |
Make rs9896933(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 82940212 |
Gene | LOC105371944, TBCD |
is a | snp |
is | mentioned by |
dbSNP | rs9896933 |
dbSNP (classic) | rs9896933 |
ClinGen | rs9896933 |
ebi | rs9896933 |
HLI | rs9896933 |
Exac | rs9896933 |
Gnomad | rs9896933 |
Varsome | rs9896933 |
LitVar | rs9896933 |
Map | rs9896933 |
PheGenI | rs9896933 |
Biobank | rs9896933 |
1000 genomes | rs9896933 |
hgdp | rs9896933 |
ensembl | rs9896933 |
geneview | rs9896933 |
scholar | rs9896933 |
rs9896933 | |
pharmgkb | rs9896933 |
gwascentral | rs9896933 |
openSNP | rs9896933 |
23andMe | rs9896933 |
SNPshot | rs9896933 |
SNPdbe | rs9896933 |
MSV3d | rs9896933 |
GWAS Ctlg | rs9896933 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26025128] Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts