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rs2911292

From SNPedia

Orientationplus
Stabilizedplus
Make rs2911292(C;C)
Make rs2911292(C;T)
Make rs2911292(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position62547042
is asnp
is mentioned by
dbSNPrs2911292
ebirs2911292
HLIrs2911292
Exacrs2911292
Varsomers2911292
Maprs2911292
PheGenIrs2911292
hapmaprs2911292
1000 genomesrs2911292
hgdprs2911292
ensemblrs2911292
gopubmedrs2911292
geneviewrs2911292
scholarrs2911292
googlers2911292
pharmgkbrs2911292
gwascentralrs2911292
openSNPrs2911292
23andMers2911292
23andMe allrs2911292
SNP Nexus

SNPshotrs2911292
SNPdbers2911292
MSV3drs2911292
GWAS Ctlgrs2911292
GMAF0.4187
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2911292
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.414062
summary