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rs7805247

From SNPedia

Orientationplus
Stabilizedplus
Make rs7805247(C;C)
Make rs7805247(C;T)
Make rs7805247(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position3070425
is asnp
is mentioned by
dbSNPrs7805247
ebirs7805247
HLIrs7805247
Exacrs7805247
Varsomers7805247
Maprs7805247
PheGenIrs7805247
hapmaprs7805247
1000 genomesrs7805247
hgdprs7805247
ensemblrs7805247
gopubmedrs7805247
geneviewrs7805247
scholarrs7805247
googlers7805247
pharmgkbrs7805247
gwascentralrs7805247
openSNPrs7805247
23andMers7805247
23andMe allrs7805247
SNP Nexus

SNPshotrs7805247
SNPdbers7805247
MSV3drs7805247
GWAS Ctlgrs7805247
GMAF0.08356
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7805247
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.929688
summary