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rs13400652

From SNPedia

Orientationplus
Stabilizedplus
Make rs13400652(C;C)
Make rs13400652(C;T)
Make rs13400652(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position122638301
is asnp
is mentioned by
dbSNPrs13400652
ebirs13400652
HLIrs13400652
Exacrs13400652
Varsomers13400652
Maprs13400652
PheGenIrs13400652
hapmaprs13400652
1000 genomesrs13400652
hgdprs13400652
ensemblrs13400652
gopubmedrs13400652
geneviewrs13400652
scholarrs13400652
googlers13400652
pharmgkbrs13400652
gwascentralrs13400652
openSNPrs13400652
23andMers13400652
23andMe allrs13400652
SNP Nexus

SNPshotrs13400652
SNPdbers13400652
MSV3drs13400652
GWAS Ctlgrs13400652
GMAF0.3765
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs13400652
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.388889
summary