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rs8056413

From SNPedia

Orientationplus
Stabilizedplus
Make rs8056413(G;G)
Make rs8056413(G;T)
Make rs8056413(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position84049045
is asnp
is mentioned by
dbSNPrs8056413
ebirs8056413
HLIrs8056413
Exacrs8056413
Varsomers8056413
Maprs8056413
PheGenIrs8056413
hapmaprs8056413
1000 genomesrs8056413
hgdprs8056413
ensemblrs8056413
gopubmedrs8056413
geneviewrs8056413
scholarrs8056413
googlers8056413
pharmgkbrs8056413
gwascentralrs8056413
openSNPrs8056413
23andMers8056413
23andMe allrs8056413
SNP Nexus

SNPshotrs8056413
SNPdbers8056413
MSV3drs8056413
GWAS Ctlgrs8056413
GMAF0.4568
Max Magnitude
? (G;G) (G;T) (T;T) 28


GET Evidence
rs8056413
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.468254
summary