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rs4742

From SNPedia

Orientationminus
Stabilizedminus
Make rs4742(C;C)
Make rs4742(C;T)
Make rs4742(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position182894535
GeneDCTD
is asnp
is mentioned by
dbSNPrs4742
ebirs4742
HLIrs4742
Exacrs4742
Varsomers4742
Maprs4742
PheGenIrs4742
hapmaprs4742
1000 genomesrs4742
hgdprs4742
ensemblrs4742
gopubmedrs4742
geneviewrs4742
scholarrs4742
googlers4742
pharmgkbrs4742
gwascentralrs4742
openSNPrs4742
23andMers4742
23andMe allrs4742
SNP Nexus

SNPshotrs4742
SNPdbers4742
MSV3drs4742
GWAS Ctlgrs4742
GMAF0.2975
Max Magnitude
? (A;A) (A;G) (G;G)


GET Evidence
rs4742
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.379903
summary