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

rs4604727

From SNPedia

Orientationplus
Stabilizedplus
Make rs4604727(C;C)
Make rs4604727(C;G)
Make rs4604727(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position172121598
GeneDNM3
is asnp
is mentioned by
dbSNPrs4604727
ebirs4604727
HLIrs4604727
Exacrs4604727
Varsomers4604727
Maprs4604727
PheGenIrs4604727
hapmaprs4604727
1000 genomesrs4604727
hgdprs4604727
ensemblrs4604727
gopubmedrs4604727
geneviewrs4604727
scholarrs4604727
googlers4604727
pharmgkbrs4604727
gwascentralrs4604727
openSNPrs4604727
23andMers4604727
23andMe allrs4604727
SNP Nexus

SNPshotrs4604727
SNPdbers4604727
MSV3drs4604727
GWAS Ctlgrs4604727
GMAF0.3122
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs4604727
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.304688
summary