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rs1035339

From SNPedia

Orientationplus
Stabilizedplus
Make rs1035339(C;C)
Make rs1035339(C;T)
Make rs1035339(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position99995928
GeneCNTN5
is asnp
is mentioned by
dbSNPrs1035339
ebirs1035339
HLIrs1035339
Exacrs1035339
Varsomers1035339
Maprs1035339
PheGenIrs1035339
hapmaprs1035339
1000 genomesrs1035339
hgdprs1035339
ensemblrs1035339
gopubmedrs1035339
geneviewrs1035339
scholarrs1035339
googlers1035339
pharmgkbrs1035339
gwascentralrs1035339
openSNPrs1035339
23andMers1035339
23andMe allrs1035339
SNP Nexus

SNPshotrs1035339
SNPdbers1035339
MSV3drs1035339
GWAS Ctlgrs1035339
GMAF0.3182
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1035339
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.382812
summary