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

rs11215936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11215936(A;A)
Make rs11215936(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116442799
is asnp
is mentioned by
dbSNPrs11215936
ebirs11215936
HLIrs11215936
Exacrs11215936
Varsomers11215936
Maprs11215936
PheGenIrs11215936
hapmaprs11215936
1000 genomesrs11215936
hgdprs11215936
ensemblrs11215936
gopubmedrs11215936
geneviewrs11215936
scholarrs11215936
googlers11215936
pharmgkbrs11215936
gwascentralrs11215936
openSNPrs11215936
23andMers11215936
23andMe allrs11215936
SNP Nexus

SNPshotrs11215936
SNPdbers11215936
MSV3drs11215936
GWAS Ctlgrs11215936
GMAF0.04867
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11215936
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0793651
summary