rs6807362
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | increased autism risk |
(C;G) | 1 | normal autism risk |
(G;G) | 2 | decreased autism risk |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 184060222 |
Gene | HTR3C |
is a | snp |
is | mentioned by |
dbSNP | rs6807362 |
dbSNP (classic) | rs6807362 |
ClinGen | rs6807362 |
ebi | rs6807362 |
HLI | rs6807362 |
Exac | rs6807362 |
Gnomad | rs6807362 |
Varsome | rs6807362 |
LitVar | rs6807362 |
Map | rs6807362 |
PheGenI | rs6807362 |
Biobank | rs6807362 |
1000 genomes | rs6807362 |
hgdp | rs6807362 |
ensembl | rs6807362 |
geneview | rs6807362 |
scholar | rs6807362 |
rs6807362 | |
pharmgkb | rs6807362 |
gwascentral | rs6807362 |
openSNP | rs6807362 |
23andMe | rs6807362 |
SNPshot | rs6807362 |
SNPdbe | rs6807362 |
MSV3d | rs6807362 |
GWAS Ctlg | rs6807362 |
GMAF | 0.4059 |
Max Magnitude | 2 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
rs6807362 is a SNP in the 5-hydroxytryptamine (serotonin) receptor 3, family member C HTR3C gene.
In a study of 97 familes with at least one individual with autism, rs6807362 was significantly associated with the disorder (p = 0.0012).[PMID 19035560]