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rs8062487

From SNPedia

Orientationplus
Stabilizedplus
Make rs8062487(C;C)
Make rs8062487(C;T)
Make rs8062487(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position60439872
is asnp
is mentioned by
dbSNPrs8062487
ebirs8062487
HLIrs8062487
Exacrs8062487
Varsomers8062487
Maprs8062487
PheGenIrs8062487
hapmaprs8062487
1000 genomesrs8062487
hgdprs8062487
ensemblrs8062487
gopubmedrs8062487
geneviewrs8062487
scholarrs8062487
googlers8062487
pharmgkbrs8062487
gwascentralrs8062487
openSNPrs8062487
23andMers8062487
23andMe allrs8062487
SNP Nexus

SNPshotrs8062487
SNPdbers8062487
MSV3drs8062487
GWAS Ctlgrs8062487
GMAF0.3687
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs8062487
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.611111
summary