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rs795009

From SNPedia

Orientationminus
Stabilizedminus
Make rs795009(A;A)
Make rs795009(A;C)
Make rs795009(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position12167171
GeneSYN2
is asnp
is mentioned by
dbSNPrs795009
ebirs795009
HLIrs795009
Exacrs795009
Varsomers795009
Maprs795009
PheGenIrs795009
hapmaprs795009
1000 genomesrs795009
hgdprs795009
ensemblrs795009
gopubmedrs795009
geneviewrs795009
scholarrs795009
googlers795009
pharmgkbrs795009
gwascentralrs795009
openSNPrs795009
23andMers795009
23andMe allrs795009
SNP Nexus

SNPshotrs795009
SNPdbers795009
MSV3drs795009
GWAS Ctlgrs795009
GMAF0.286
Max Magnitude
? (A;A) (A;C) (C;C) 28
rs795009 and rs310762 have been linked to schizophrenia
OMIM181500
DescSCHIZOPHRENIA; SCZD
Variant
Relatedalso
OMIM600755
DescSYNAPSIN II; SYN2
Variant
Relatedalso


[PMID 15271586] Positive association between synapsin II and schizophrenia.


[PMID 15449241OA-icon.png] Family-based association study of synapsin II and schizophrenia.


[PMID 16131404OA-icon.png] Association study of polymorphisms in synaptic vesicle-associated genes, SYN2 and CPLX2, with schizophrenia.


[PMID 17766091OA-icon.png] Association of synapsin 2 with schizophrenia in families of Northern European ancestry.