Have questions? Visit https://www.reddit.com/r/SNPedia

rs3864671

From SNPedia

Orientationplus
Stabilizedplus
Make rs3864671(C;C)
Make rs3864671(C;T)
Make rs3864671(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position61240490
is asnp
is mentioned by
dbSNPrs3864671
ebirs3864671
HLIrs3864671
Exacrs3864671
Varsomers3864671
Maprs3864671
PheGenIrs3864671
hapmaprs3864671
1000 genomesrs3864671
hgdprs3864671
ensemblrs3864671
gopubmedrs3864671
geneviewrs3864671
scholarrs3864671
googlers3864671
pharmgkbrs3864671
gwascentralrs3864671
openSNPrs3864671
23andMers3864671
23andMe allrs3864671
SNP Nexus

SNPshotrs3864671
SNPdbers3864671
MSV3drs3864671
GWAS Ctlgrs3864671
GMAF0.292
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs3864671
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.28125
summary