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

rs6966038

From SNPedia

Orientationplus
Stabilizedplus
Make rs6966038(A;A)
Make rs6966038(A;G)
Make rs6966038(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position157087704
GeneLOC645272
is asnp
is mentioned by
dbSNPrs6966038
ebirs6966038
HLIrs6966038
Exacrs6966038
Varsomers6966038
Maprs6966038
PheGenIrs6966038
hapmaprs6966038
1000 genomesrs6966038
hgdprs6966038
ensemblrs6966038
gopubmedrs6966038
geneviewrs6966038
scholarrs6966038
googlers6966038
pharmgkbrs6966038
gwascentralrs6966038
openSNPrs6966038
23andMers6966038
23andMe allrs6966038
SNP Nexus

SNPshotrs6966038
SNPdbers6966038
MSV3drs6966038
GWAS Ctlgrs6966038
GMAF0.2199
Max Magnitude
? (A;A) (A;G) (G;G) 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 5E-7
Odds Ratio 1.64 [1.35-1.99]


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


GET Evidence
rs6966038
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary