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rs11226029

From SNPedia
Orientationplus
Stabilizedplus
Make rs11226029(A;A)
Make rs11226029(A;G)
Make rs11226029(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position103822899
is asnp
is mentioned by
dbSNPrs11226029
dbSNP (old)rs11226029
ClinGenrs11226029
ebirs11226029
HLIrs11226029
Exacrs11226029
Gnomadrs11226029
Varsomers11226029
Maprs11226029
PheGenIrs11226029
Biobankrs11226029
1000 genomesrs11226029
hgdprs11226029
ensemblrs11226029
gopubmedrs11226029
geneviewrs11226029
scholarrs11226029
googlers11226029
pharmgkbrs11226029
gwascentralrs11226029
openSNPrs11226029
23andMers11226029
23andMe allrs11226029
SNPshotrs11226029
SNPdbers11226029
MSV3drs11226029
GWAS Ctlgrs11226029
Max Magnitude
? (A;A) (A;G) (G;G) 28
Named in 10.1056/NEJMoa1605086 as a SNP potentially used in the calculation of a cardiovascular genetic risk score