rs10103692
From SNPedia
Orientation | plus |
Make rs10103692(A;A) |
Make rs10103692(A;G) |
Make rs10103692(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 8 |
Position | 54345567 |
is a | snp |
is | mentioned by |
dbSNP | rs10103692 |
dbSNP (classic) | rs10103692 |
ClinGen | rs10103692 |
ebi | rs10103692 |
HLI | rs10103692 |
Exac | rs10103692 |
Gnomad | rs10103692 |
Varsome | rs10103692 |
LitVar | rs10103692 |
Map | rs10103692 |
PheGenI | rs10103692 |
Biobank | rs10103692 |
1000 genomes | rs10103692 |
hgdp | rs10103692 |
ensembl | rs10103692 |
geneview | rs10103692 |
scholar | rs10103692 |
rs10103692 | |
pharmgkb | rs10103692 |
gwascentral | rs10103692 |
openSNP | rs10103692 |
23andMe | rs10103692 |
SNPshot | rs10103692 |
SNPdbe | rs10103692 |
MSV3d | rs10103692 |
GWAS Ctlg | rs10103692 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30527956] Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis;
odds ratio 1·80 [95% CI 1·55-2·08], p=5·13 × 10e-15