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rs3909276

From SNPedia

Orientationminus
Stabilizedminus
Make rs3909276(C;C)
Make rs3909276(C;T)
Make rs3909276(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position100007484
GeneCNTN5
is asnp
is mentioned by
dbSNPrs3909276
ebirs3909276
HLIrs3909276
Exacrs3909276
Varsomers3909276
Maprs3909276
PheGenIrs3909276
hapmaprs3909276
1000 genomesrs3909276
hgdprs3909276
ensemblrs3909276
gopubmedrs3909276
geneviewrs3909276
scholarrs3909276
googlers3909276
pharmgkbrs3909276
gwascentralrs3909276
openSNPrs3909276
23andMers3909276
23andMe allrs3909276
SNP Nexus

SNPshotrs3909276
SNPdbers3909276
MSV3drs3909276
GWAS Ctlgrs3909276
GMAF0.3219
Max Magnitude
? (C;C) (C;T) (T;T) 28
GET Evidence
rs3909276
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.382812
summary