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

rs11636705

From SNPedia

Orientationplus
Stabilizedplus
Make rs11636705(C;C)
Make rs11636705(C;T)
Make rs11636705(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position96062683
is asnp
is mentioned by
dbSNPrs11636705
ebirs11636705
HLIrs11636705
Exacrs11636705
Varsomers11636705
Maprs11636705
PheGenIrs11636705
hapmaprs11636705
1000 genomesrs11636705
hgdprs11636705
ensemblrs11636705
gopubmedrs11636705
geneviewrs11636705
scholarrs11636705
googlers11636705
pharmgkbrs11636705
gwascentralrs11636705
openSNPrs11636705
23andMers11636705
23andMe allrs11636705
SNP Nexus

SNPshotrs11636705
SNPdbers11636705
MSV3drs11636705
GWAS Ctlgrs11636705
GMAF0.146
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11636705
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.140625
summary