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rs3769376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3769376(C;C)
Make rs3769376(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position157421733
GeneCYTIP
is asnp
is mentioned by
dbSNPrs3769376
ebirs3769376
HLIrs3769376
Exacrs3769376
Varsomers3769376
Maprs3769376
PheGenIrs3769376
hapmaprs3769376
1000 genomesrs3769376
hgdprs3769376
ensemblrs3769376
gopubmedrs3769376
geneviewrs3769376
scholarrs3769376
googlers3769376
pharmgkbrs3769376
gwascentralrs3769376
openSNPrs3769376
23andMers3769376
23andMe allrs3769376
SNP Nexus

SNPshotrs3769376
SNPdbers3769376
MSV3drs3769376
GWAS Ctlgrs3769376
GMAF0.04959
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs3769376
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0546875
summary