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rs327127

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs327127(C;G)
Make rs327127(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position28944763
is asnp
is mentioned by
dbSNPrs327127
ebirs327127
HLIrs327127
Exacrs327127
Varsomers327127
Maprs327127
PheGenIrs327127
hapmaprs327127
1000 genomesrs327127
hgdprs327127
ensemblrs327127
gopubmedrs327127
geneviewrs327127
scholarrs327127
googlers327127
pharmgkbrs327127
gwascentralrs327127
openSNPrs327127
23andMers327127
23andMe allrs327127
SNP Nexus

SNPshotrs327127
SNPdbers327127
MSV3drs327127
GWAS Ctlgrs327127
GMAF0.1589
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs327127
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.835938
summary