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

rs6007413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6007413(C;G)
Make rs6007413(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position45034435
is asnp
is mentioned by
dbSNPrs6007413
ebirs6007413
HLIrs6007413
Exacrs6007413
Varsomers6007413
Maprs6007413
PheGenIrs6007413
hapmaprs6007413
1000 genomesrs6007413
hgdprs6007413
ensemblrs6007413
gopubmedrs6007413
geneviewrs6007413
scholarrs6007413
googlers6007413
pharmgkbrs6007413
gwascentralrs6007413
openSNPrs6007413
23andMers6007413
23andMe allrs6007413
SNP Nexus

SNPshotrs6007413
SNPdbers6007413
MSV3drs6007413
GWAS Ctlgrs6007413
GMAF0.2199
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs6007413
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.164062
summary