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rs389719

From SNPedia

Orientationminus
Stabilizedplus
Make rs389719(C;C)
Make rs389719(C;T)
Make rs389719(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position27957331
is asnp
is mentioned by
dbSNPrs389719
ebirs389719
HLIrs389719
Exacrs389719
Varsomers389719
Maprs389719
PheGenIrs389719
hapmaprs389719
1000 genomesrs389719
hgdprs389719
ensemblrs389719
gopubmedrs389719
geneviewrs389719
scholarrs389719
googlers389719
pharmgkbrs389719
gwascentralrs389719
openSNPrs389719
23andMers389719
23andMe allrs389719
SNP Nexus

SNPshotrs389719
SNPdbers389719
MSV3drs389719
GWAS Ctlgrs389719
GMAF0.3122
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs389719
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary