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rs2289015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2289015(A;A)
Make rs2289015(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position54609389
GeneACOT11, FAM151A
is asnp
is mentioned by
dbSNPrs2289015
ebirs2289015
HLIrs2289015
Exacrs2289015
Varsomers2289015
Maprs2289015
PheGenIrs2289015
hapmaprs2289015
1000 genomesrs2289015
hgdprs2289015
ensemblrs2289015
gopubmedrs2289015
geneviewrs2289015
scholarrs2289015
googlers2289015
pharmgkbrs2289015
gwascentralrs2289015
openSNPrs2289015
23andMers2289015
23andMe allrs2289015
SNP Nexus

SNPshotrs2289015
SNPdbers2289015
MSV3drs2289015
GWAS Ctlgrs2289015
GMAF0.0877
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
FAM151A-G546D
aa_change Gly546Asp
aa_change_short G546D
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0318832
summary