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rs1425967

From SNPedia

Orientationminus
Stabilizedminus
Make rs1425967(C;C)
Make rs1425967(C;T)
Make rs1425967(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position137367736
is asnp
is mentioned by
dbSNPrs1425967
ebirs1425967
HLIrs1425967
Exacrs1425967
Varsomers1425967
Maprs1425967
PheGenIrs1425967
hapmaprs1425967
1000 genomesrs1425967
hgdprs1425967
ensemblrs1425967
gopubmedrs1425967
geneviewrs1425967
scholarrs1425967
googlers1425967
pharmgkbrs1425967
gwascentralrs1425967
openSNPrs1425967
23andMers1425967
23andMe allrs1425967
SNP Nexus

SNPshotrs1425967
SNPdbers1425967
MSV3drs1425967
GWAS Ctlgrs1425967
GMAF0.4564
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1425967
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.578125
summary