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rs787151

From SNPedia

Orientationminus
Stabilizedminus
Make rs787151(C;C)
Make rs787151(C;T)
Make rs787151(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position143898268
is asnp
is mentioned by
dbSNPrs787151
ebirs787151
HLIrs787151
Exacrs787151
Varsomers787151
Maprs787151
PheGenIrs787151
hapmaprs787151
1000 genomesrs787151
hgdprs787151
ensemblrs787151
gopubmedrs787151
geneviewrs787151
scholarrs787151
googlers787151
pharmgkbrs787151
gwascentralrs787151
openSNPrs787151
23andMers787151
23andMe allrs787151
SNP Nexus

SNPshotrs787151
SNPdbers787151
MSV3drs787151
GWAS Ctlgrs787151
GMAF0.1846
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs787151
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.796875
summary