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rs17252296

From SNPedia

Orientationplus
Stabilizedplus
Make rs17252296(A;A)
Make rs17252296(A;C)
Make rs17252296(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position51114203
is asnp
is mentioned by
dbSNPrs17252296
ebirs17252296
HLIrs17252296
Exacrs17252296
Varsomers17252296
Maprs17252296
PheGenIrs17252296
hapmaprs17252296
1000 genomesrs17252296
hgdprs17252296
ensemblrs17252296
gopubmedrs17252296
geneviewrs17252296
scholarrs17252296
googlers17252296
pharmgkbrs17252296
gwascentralrs17252296
openSNPrs17252296
23andMers17252296
23andMe allrs17252296
SNP Nexus

SNPshotrs17252296
SNPdbers17252296
MSV3drs17252296
GWAS Ctlgrs17252296
GMAF0.1598
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs17252296
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.140625
summary