rs795009
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs795009(A;A) |
Make rs795009(A;C) |
Make rs795009(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 12167171 |
Gene | SYN2 |
is a | snp |
is | mentioned by |
dbSNP | rs795009 |
dbSNP (classic) | rs795009 |
ClinGen | rs795009 |
ebi | rs795009 |
HLI | rs795009 |
Exac | rs795009 |
Gnomad | rs795009 |
Varsome | rs795009 |
LitVar | rs795009 |
Map | rs795009 |
PheGenI | rs795009 |
Biobank | rs795009 |
1000 genomes | rs795009 |
hgdp | rs795009 |
ensembl | rs795009 |
geneview | rs795009 |
scholar | rs795009 |
rs795009 | |
pharmgkb | rs795009 |
gwascentral | rs795009 |
openSNP | rs795009 |
23andMe | rs795009 |
SNPshot | rs795009 |
SNPdbe | rs795009 |
MSV3d | rs795009 |
GWAS Ctlg | rs795009 |
GMAF | 0.286 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
rs795009 and rs310762 have been linked to schizophrenia
[PMID 15271586] Positive association between synapsin II and schizophrenia.
[PMID 15449241] Family-based association study of synapsin II and schizophrenia.
[PMID 16131404] Association study of polymorphisms in synaptic vesicle-associated genes, SYN2 and CPLX2, with schizophrenia.
[PMID 17766091] Association of synapsin 2 with schizophrenia in families of Northern European ancestry.