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rs11082277

From SNPedia

Orientationplus
Stabilizedplus
Make rs11082277(A;A)
Make rs11082277(A;G)
Make rs11082277(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position42470398
GeneCENPW
is asnp
is mentioned by
dbSNPrs11082277
ebirs11082277
HLIrs11082277
Exacrs11082277
Varsomers11082277
Maprs11082277
PheGenIrs11082277
hapmaprs11082277
1000 genomesrs11082277
hgdprs11082277
ensemblrs11082277
gopubmedrs11082277
geneviewrs11082277
scholarrs11082277
googlers11082277
pharmgkbrs11082277
gwascentralrs11082277
openSNPrs11082277
23andMers11082277
23andMe allrs11082277
SNP Nexus

SNPshotrs11082277
SNPdbers11082277
MSV3drs11082277
GWAS Ctlgrs11082277
GMAF0.3177
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11082277
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.421875
summary