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rs6484176

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6484176(C;C)
Make rs6484176(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position25766084
is asnp
is mentioned by
dbSNPrs6484176
ebirs6484176
HLIrs6484176
Exacrs6484176
Varsomers6484176
Maprs6484176
PheGenIrs6484176
hapmaprs6484176
1000 genomesrs6484176
hgdprs6484176
ensemblrs6484176
gopubmedrs6484176
geneviewrs6484176
scholarrs6484176
googlers6484176
pharmgkbrs6484176
gwascentralrs6484176
openSNPrs6484176
23andMers6484176
23andMe allrs6484176
SNP Nexus

SNPshotrs6484176
SNPdbers6484176
MSV3drs6484176
GWAS Ctlgrs6484176
GMAF0.2544
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6484176
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.367188
summary