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rs11222291

From SNPedia

Orientationplus
Stabilizedplus
Make rs11222291(C;C)
Make rs11222291(C;T)
Make rs11222291(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position100002814
GeneCNTN5
is asnp
is mentioned by
dbSNPrs11222291
ebirs11222291
HLIrs11222291
Exacrs11222291
Varsomers11222291
Maprs11222291
PheGenIrs11222291
hapmaprs11222291
1000 genomesrs11222291
hgdprs11222291
ensemblrs11222291
gopubmedrs11222291
geneviewrs11222291
scholarrs11222291
googlers11222291
pharmgkbrs11222291
gwascentralrs11222291
openSNPrs11222291
23andMers11222291
23andMe allrs11222291
SNP Nexus

SNPshotrs11222291
SNPdbers11222291
MSV3drs11222291
GWAS Ctlgrs11222291
GMAF0.3255
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs11222291
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.388889
summary