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

rs4269885

From SNPedia

Orientationplus
Stabilizedplus
Make rs4269885(A;A)
Make rs4269885(A;G)
Make rs4269885(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position99994817
GeneCNTN5
is asnp
is mentioned by
dbSNPrs4269885
ebirs4269885
HLIrs4269885
Exacrs4269885
Varsomers4269885
Maprs4269885
PheGenIrs4269885
hapmaprs4269885
1000 genomesrs4269885
hgdprs4269885
ensemblrs4269885
gopubmedrs4269885
geneviewrs4269885
scholarrs4269885
googlers4269885
pharmgkbrs4269885
gwascentralrs4269885
openSNPrs4269885
23andMers4269885
23andMe allrs4269885
SNP Nexus

SNPshotrs4269885
SNPdbers4269885
MSV3drs4269885
GWAS Ctlgrs4269885
GMAF0.4573
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs4269885
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.442623
summary