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

rs11673011

From SNPedia

Orientationplus
Stabilizedplus
Make rs11673011(A;A)
Make rs11673011(A;G)
Make rs11673011(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34124178
is asnp
is mentioned by
dbSNPrs11673011
ebirs11673011
HLIrs11673011
Exacrs11673011
Varsomers11673011
Maprs11673011
PheGenIrs11673011
hapmaprs11673011
1000 genomesrs11673011
hgdprs11673011
ensemblrs11673011
gopubmedrs11673011
geneviewrs11673011
scholarrs11673011
googlers11673011
pharmgkbrs11673011
gwascentralrs11673011
openSNPrs11673011
23andMers11673011
23andMe allrs11673011
SNP Nexus

SNPshotrs11673011
SNPdbers11673011
MSV3drs11673011
GWAS Ctlgrs11673011
GMAF0.2686
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11673011
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary