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rs6590495

From SNPedia

Orientationplus
Stabilizedplus
Make rs6590495(C;C)
Make rs6590495(C;T)
Make rs6590495(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position99996266
GeneCNTN5
is asnp
is mentioned by
dbSNPrs6590495
ebirs6590495
HLIrs6590495
Exacrs6590495
Varsomers6590495
Maprs6590495
PheGenIrs6590495
hapmaprs6590495
1000 genomesrs6590495
hgdprs6590495
ensemblrs6590495
gopubmedrs6590495
geneviewrs6590495
scholarrs6590495
googlers6590495
pharmgkbrs6590495
gwascentralrs6590495
openSNPrs6590495
23andMers6590495
23andMe allrs6590495
SNP Nexus

SNPshotrs6590495
SNPdbers6590495
MSV3drs6590495
GWAS Ctlgrs6590495
GMAF0.3255
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6590495
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary