Have questions? Visit https://www.reddit.com/r/SNPedia

rs165849

From SNPedia

Orientationplus
Stabilizedplus
Make rs165849(A;A)
Make rs165849(A;G)
Make rs165849(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19971146
GeneARVCF
is asnp
is mentioned by
dbSNPrs165849
ebirs165849
HLIrs165849
Exacrs165849
Varsomers165849
Maprs165849
PheGenIrs165849
hapmaprs165849
1000 genomesrs165849
hgdprs165849
ensemblrs165849
gopubmedrs165849
geneviewrs165849
scholarrs165849
googlers165849
pharmgkbrs165849
gwascentralrs165849
openSNPrs165849
23andMers165849
23andMe allrs165849
SNP Nexus

SNPshotrs165849
SNPdbers165849
MSV3drs165849
GWAS Ctlgrs165849
GMAF0.4803
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20333729OA-icon.png] A functional variant provided further evidence for the association of ARVCF with schizophrenia


[PMID 19508883] ARVCF single marker and haplotypic association with schizophrenia


[PMID 15340358] Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.


[PMID 16232322OA-icon.png] COMT genetic variation confers risk for psychotic and affective disorders: a case control study.


[PMID 19015200OA-icon.png] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.


[PMID 19329282] Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.