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

rs11067600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11067600(C;C)
Make rs11067600(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position115439972
is asnp
is mentioned by
dbSNPrs11067600
ebirs11067600
HLIrs11067600
Exacrs11067600
Varsomers11067600
Maprs11067600
PheGenIrs11067600
hapmaprs11067600
1000 genomesrs11067600
hgdprs11067600
ensemblrs11067600
gopubmedrs11067600
geneviewrs11067600
scholarrs11067600
googlers11067600
pharmgkbrs11067600
gwascentralrs11067600
openSNPrs11067600
23andMers11067600
23andMe allrs11067600
SNP Nexus

SNPshotrs11067600
SNPdbers11067600
MSV3drs11067600
GWAS Ctlgrs11067600
GMAF0.1983
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11067600
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.1875
summary