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rs12941878

From SNPedia

Orientationplus
Stabilizedplus
Make rs12941878(A;A)
Make rs12941878(A;G)
Make rs12941878(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position55382944
is asnp
is mentioned by
dbSNPrs12941878
ebirs12941878
HLIrs12941878
Exacrs12941878
Varsomers12941878
Maprs12941878
PheGenIrs12941878
hapmaprs12941878
1000 genomesrs12941878
hgdprs12941878
ensemblrs12941878
gopubmedrs12941878
geneviewrs12941878
scholarrs12941878
googlers12941878
pharmgkbrs12941878
gwascentralrs12941878
openSNPrs12941878
23andMers12941878
23andMe allrs12941878
SNP Nexus

SNPshotrs12941878
SNPdbers12941878
MSV3drs12941878
GWAS Ctlgrs12941878
GMAF0.2755
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs12941878
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.75
summary