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rs3864670

From SNPedia

Orientationplus
Stabilizedplus
Make rs3864670(A;A)
Make rs3864670(A;G)
Make rs3864670(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position61240342
is asnp
is mentioned by
dbSNPrs3864670
ebirs3864670
HLIrs3864670
Exacrs3864670
Varsomers3864670
Maprs3864670
PheGenIrs3864670
hapmaprs3864670
1000 genomesrs3864670
hgdprs3864670
ensemblrs3864670
gopubmedrs3864670
geneviewrs3864670
scholarrs3864670
googlers3864670
pharmgkbrs3864670
gwascentralrs3864670
openSNPrs3864670
23andMers3864670
23andMe allrs3864670
SNP Nexus

SNPshotrs3864670
SNPdbers3864670
MSV3drs3864670
GWAS Ctlgrs3864670
GMAF0.292
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs3864670
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.28125
summary