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rs6127921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6127921(A;C)
Make rs6127921(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position57063694
is asnp
is mentioned by
dbSNPrs6127921
ebirs6127921
HLIrs6127921
Exacrs6127921
Varsomers6127921
Maprs6127921
PheGenIrs6127921
hapmaprs6127921
1000 genomesrs6127921
hgdprs6127921
ensemblrs6127921
gopubmedrs6127921
geneviewrs6127921
scholarrs6127921
googlers6127921
pharmgkbrs6127921
gwascentralrs6127921
openSNPrs6127921
23andMers6127921
23andMe allrs6127921
SNP Nexus

SNPshotrs6127921
SNPdbers6127921
MSV3drs6127921
GWAS Ctlgrs6127921
GMAF0.2447
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19846067OA-icon.png]
Trait Treatment response to citalopram
Title A Genomewide Association Study of Citalopram Response in Major Depressive Disorder
Risk Allele
P-val 0.000003
Odds Ratio 1.64 [1.33-2.04]

[PMID 21172166OA-icon.png] Pharmacogenetics of antidepressant response.


GET Evidence
rs6127921
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary