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rs11222869

From SNPedia

Orientationplus
Stabilizedplus
Make rs11222869(A;A)
Make rs11222869(A;G)
Make rs11222869(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position132031854
GeneNTM
is asnp
is mentioned by
dbSNPrs11222869
ebirs11222869
HLIrs11222869
Exacrs11222869
Varsomers11222869
Maprs11222869
PheGenIrs11222869
hapmaprs11222869
1000 genomesrs11222869
hgdprs11222869
ensemblrs11222869
gopubmedrs11222869
geneviewrs11222869
scholarrs11222869
googlers11222869
pharmgkbrs11222869
gwascentralrs11222869
openSNPrs11222869
23andMers11222869
23andMe allrs11222869
SNP Nexus

SNPshotrs11222869
SNPdbers11222869
MSV3drs11222869
GWAS Ctlgrs11222869
GMAF0.4982
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11222869
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.46875
summary