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

rs6481464

From SNPedia

Orientationplus
Stabilizedplus
Make rs6481464(C;C)
Make rs6481464(C;T)
Make rs6481464(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position59360724
GeneFAM13C
is asnp
is mentioned by
dbSNPrs6481464
ebirs6481464
HLIrs6481464
Exacrs6481464
Varsomers6481464
Maprs6481464
PheGenIrs6481464
hapmaprs6481464
1000 genomesrs6481464
hgdprs6481464
ensemblrs6481464
gopubmedrs6481464
geneviewrs6481464
scholarrs6481464
googlers6481464
pharmgkbrs6481464
gwascentralrs6481464
openSNPrs6481464
23andMers6481464
23andMe allrs6481464
SNP Nexus

SNPshotrs6481464
SNPdbers6481464
MSV3drs6481464
GWAS Ctlgrs6481464
GMAF0.3411
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6481464
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.289062
summary