Have questions? Visit https://www.reddit.com/r/SNPedia

rs4673727

From SNPedia

Orientationplus
Stabilizedplus
Make rs4673727(C;C)
Make rs4673727(C;T)
Make rs4673727(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position200130964
is asnp
is mentioned by
dbSNPrs4673727
ebirs4673727
HLIrs4673727
Exacrs4673727
Varsomers4673727
Maprs4673727
PheGenIrs4673727
hapmaprs4673727
1000 genomesrs4673727
hgdprs4673727
ensemblrs4673727
gopubmedrs4673727
geneviewrs4673727
scholarrs4673727
googlers4673727
pharmgkbrs4673727
gwascentralrs4673727
openSNPrs4673727
23andMers4673727
23andMe allrs4673727
SNP Nexus

SNPshotrs4673727
SNPdbers4673727
MSV3drs4673727
GWAS Ctlgrs4673727
GMAF0.1455
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4673727
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.8125
summary