Have questions? Visit https://www.reddit.com/r/SNPedia

rs10811656

From SNPedia

Orientationplus
Make rs10811656(C;C)
Make rs10811656(C;T)
Make rs10811656(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position22124473
is asnp
is mentioned by
dbSNPrs10811656
ebirs10811656
HLIrs10811656
Exacrs10811656
Varsomers10811656
Maprs10811656
PheGenIrs10811656
hapmaprs10811656
1000 genomesrs10811656
hgdprs10811656
ensemblrs10811656
gopubmedrs10811656
geneviewrs10811656
scholarrs10811656
googlers10811656
pharmgkbrs10811656
gwascentralrs10811656
openSNPrs10811656
23andMers10811656
23andMe allrs10811656
SNP Nexus

SNPshotrs10811656
SNPdbers10811656
MSV3drs10811656
GWAS Ctlgrs10811656
Max Magnitude

[PMID 27507036] Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese population.