Have questions? Visit https://www.reddit.com/r/SNPedia

rs6590489

From SNPedia

Orientationplus
Stabilizedplus
Make rs6590489(C;C)
Make rs6590489(C;T)
Make rs6590489(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position99993043
GeneCNTN5
is asnp
is mentioned by
dbSNPrs6590489
ebirs6590489
HLIrs6590489
Exacrs6590489
Varsomers6590489
Maprs6590489
PheGenIrs6590489
hapmaprs6590489
1000 genomesrs6590489
hgdprs6590489
ensemblrs6590489
gopubmedrs6590489
geneviewrs6590489
scholarrs6590489
googlers6590489
pharmgkbrs6590489
gwascentralrs6590489
openSNPrs6590489
23andMers6590489
23andMe allrs6590489
SNP Nexus

SNPshotrs6590489
SNPdbers6590489
MSV3drs6590489
GWAS Ctlgrs6590489
GMAF0.3255
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6590489
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary