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

rs1377580

From SNPedia

Orientationplus
Stabilizedplus
Make rs1377580(C;C)
Make rs1377580(C;T)
Make rs1377580(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position99995431
GeneCNTN5
is asnp
is mentioned by
dbSNPrs1377580
ebirs1377580
HLIrs1377580
Exacrs1377580
Varsomers1377580
Maprs1377580
PheGenIrs1377580
hapmaprs1377580
1000 genomesrs1377580
hgdprs1377580
ensemblrs1377580
gopubmedrs1377580
geneviewrs1377580
scholarrs1377580
googlers1377580
pharmgkbrs1377580
gwascentralrs1377580
openSNPrs1377580
23andMers1377580
23andMe allrs1377580
SNP Nexus

SNPshotrs1377580
SNPdbers1377580
MSV3drs1377580
GWAS Ctlgrs1377580
GMAF0.3264
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1377580
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary