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rs16861531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16861531(C;C)
Make rs16861531(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position14257928
GeneLINC00276
is asnp
is mentioned by
dbSNPrs16861531
ebirs16861531
HLIrs16861531
Exacrs16861531
Varsomers16861531
Maprs16861531
PheGenIrs16861531
hapmaprs16861531
1000 genomesrs16861531
hgdprs16861531
ensemblrs16861531
gopubmedrs16861531
geneviewrs16861531
scholarrs16861531
googlers16861531
pharmgkbrs16861531
gwascentralrs16861531
openSNPrs16861531
23andMers16861531
23andMe allrs16861531
SNP Nexus

SNPshotrs16861531
SNPdbers16861531
MSV3drs16861531
GWAS Ctlgrs16861531
GMAF0.04867
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22041458OA-icon.png]
Trait
Title Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.
Risk Allele G
P-val 7E-7
Odds Ratio None None