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rs16965628

From SNPedia

Orientationplus
Stabilizedplus
Make rs16965628(C;C)
Make rs16965628(C;G)
Make rs16965628(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position30228407
GeneSLC6A4
is asnp
is mentioned by
dbSNPrs16965628
ebirs16965628
HLIrs16965628
Exacrs16965628
Varsomers16965628
Maprs16965628
PheGenIrs16965628
hapmaprs16965628
1000 genomesrs16965628
hgdprs16965628
ensemblrs16965628
gopubmedrs16965628
geneviewrs16965628
scholarrs16965628
googlers16965628
pharmgkbrs16965628
gwascentralrs16965628
openSNPrs16965628
23andMers16965628
23andMe allrs16965628
SNP Nexus

SNPshotrs16965628
SNPdbers16965628
MSV3drs16965628
GWAS Ctlgrs16965628
GMAF0.1267
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 22594806OA-icon.png] Association between a genetic variant in the serotonin transporter gene (SLC6A4) and suicidal behavior in patients with schizophrenia


[PMID 18055562] A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorder.


[PMID 18444253OA-icon.png] Additional functional variation at the SLC6A4 gene.


[PMID 18824000OA-icon.png] How the serotonin story is being rewritten by new gene-based discoveries principally related to SLC6A4, the serotonin transporter gene, which functions to influence all cellular serotonin systems.


[PMID 18937309OA-icon.png] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.


[PMID 19860858OA-icon.png] Combinatorial interaction between two human serotonin transporter gene variable number tandem repeats and their regulation by CTCF.