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rs17682547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs17682547(C;C)
Make rs17682547(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position3395801
is asnp
is mentioned by
dbSNPrs17682547
ClinGenrs17682547
ebirs17682547
HLIrs17682547
Exacrs17682547
Varsomers17682547
Maprs17682547
PheGenIrs17682547
hapmaprs17682547
1000 genomesrs17682547
hgdprs17682547
ensemblrs17682547
gopubmedrs17682547
geneviewrs17682547
scholarrs17682547
googlers17682547
pharmgkbrs17682547
gwascentralrs17682547
openSNPrs17682547
23andMers17682547
23andMe allrs17682547
SNP Nexus

SNPshotrs17682547
SNPdbers17682547
MSV3drs17682547
GWAS Ctlgrs17682547
GMAF0.02663
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs17682547
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.015625
summary