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rs10103692

From SNPedia

Orientationplus
Make rs10103692(A;A)
Make rs10103692(A;G)
Make rs10103692(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome8
Position54345567
is asnp
is mentioned by
dbSNPrs10103692
dbSNP (classic)rs10103692
ClinGenrs10103692
ebirs10103692
HLIrs10103692
Exacrs10103692
Gnomadrs10103692
Varsomers10103692
LitVarrs10103692
Maprs10103692
PheGenIrs10103692
Biobankrs10103692
1000 genomesrs10103692
hgdprs10103692
ensemblrs10103692
geneviewrs10103692
scholarrs10103692
googlers10103692
pharmgkbrs10103692
gwascentralrs10103692
openSNPrs10103692
23andMers10103692
23andMe allrs10103692
SNPshotrs10103692
SNPdbers10103692
MSV3drs10103692
GWAS Ctlgrs10103692
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 30527956OA-icon.png] 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