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rs1486649

From SNPedia

Orientationminus
Stabilizedminus
Make rs1486649(G;G)
Make rs1486649(G;T)
Make rs1486649(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position61235436
is asnp
is mentioned by
dbSNPrs1486649
ebirs1486649
HLIrs1486649
Exacrs1486649
Varsomers1486649
Maprs1486649
PheGenIrs1486649
hapmaprs1486649
1000 genomesrs1486649
hgdprs1486649
ensemblrs1486649
gopubmedrs1486649
geneviewrs1486649
scholarrs1486649
googlers1486649
pharmgkbrs1486649
gwascentralrs1486649
openSNPrs1486649
23andMers1486649
23andMe allrs1486649
SNP Nexus

SNPshotrs1486649
SNPdbers1486649
MSV3drs1486649
GWAS Ctlgrs1486649
GMAF0.292
Max Magnitude
? (G;G) (G;T) (T;T) 28


GET Evidence
rs1486649
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.28125
summary