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rs28914832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs28914832(A;G)
Make rs28914832(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position30211356
GeneSLC6A4
is asnp
is mentioned by
dbSNPrs28914832
ebirs28914832
HLIrs28914832
Exacrs28914832
Varsomers28914832
Maprs28914832
PheGenIrs28914832
hapmaprs28914832
1000 genomesrs28914832
hgdprs28914832
ensemblrs28914832
gopubmedrs28914832
geneviewrs28914832
scholarrs28914832
googlers28914832
pharmgkbrs28914832
gwascentralrs28914832
openSNPrs28914832
23andMers28914832
23andMe allrs28914832
SNP Nexus

SNPshotrs28914832
SNPdbers28914832
MSV3drs28914832
GWAS Ctlgrs28914832
Max Magnitude0
OMIM182138
Desc
Variant0002
Relatedalso


ClinVar
Risk rs28914832(C,G;C,G)
Alt rs28914832(C,G;C,G)
Reference rs28914832(A;A)
Significance Other
Disease Obsessive-compulsive disorder
Variation info
Gene SLC6A4
CLNDBN Obsessive-compulsive disorder, susceptibility to
Reversed 1
HGVS NC_000017.10:g.28538374T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013798.2,



[PMID 15995945OA-icon.png] Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

[PMID 18957375OA-icon.png] Enhanced activity of human serotonin transporter variants associated with autism.

[PMID 19032574OA-icon.png] Characterization of a functional polymorphism in the 3' UTR of SLC6A4 and its association with drinking intensity.