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rs1833489

From SNPedia

Orientationplus
Stabilizedplus
Make rs1833489(C;C)
Make rs1833489(C;T)
Make rs1833489(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position100001440
GeneCNTN5
is asnp
is mentioned by
dbSNPrs1833489
ebirs1833489
HLIrs1833489
Exacrs1833489
Varsomers1833489
Maprs1833489
PheGenIrs1833489
hapmaprs1833489
1000 genomesrs1833489
hgdprs1833489
ensemblrs1833489
gopubmedrs1833489
geneviewrs1833489
scholarrs1833489
googlers1833489
pharmgkbrs1833489
gwascentralrs1833489
openSNPrs1833489
23andMers1833489
23andMe allrs1833489
SNP Nexus

SNPshotrs1833489
SNPdbers1833489
MSV3drs1833489
GWAS Ctlgrs1833489
GMAF0.3287
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1833489
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.40625
summary