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rs17727261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17727261(C;T)
Make rs17727261(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position124524333
GeneCNTNAP5
is asnp
is mentioned by
dbSNPrs17727261
dbSNP (old)rs17727261
ClinGenrs17727261
ebirs17727261
HLIrs17727261
Exacrs17727261
Gnomadrs17727261
Varsomers17727261
Maprs17727261
PheGenIrs17727261
Biobankrs17727261
1000 genomesrs17727261
hgdprs17727261
ensemblrs17727261
gopubmedrs17727261
geneviewrs17727261
scholarrs17727261
googlers17727261
pharmgkbrs17727261
gwascentralrs17727261
openSNPrs17727261
23andMers17727261
23andMe allrs17727261
SNP Nexus

SNPshotrs17727261
SNPdbers17727261
MSV3drs17727261
GWAS Ctlgrs17727261
GMAF0.02663
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19721433OA-icon.png]
Trait Treatment response to antipsychotics
Title Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics
Risk Allele
P-val 5E-7
Odds Ratio 10.00 [NR] % of variance explained


GET Evidence
CNTNAP5-S452L
aa_change Ser452Leu
aa_change_short S452L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.03765
summary