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rs165815

From SNPedia

Orientationplus
Stabilizedplus
Make rs165815(C;C)
Make rs165815(C;T)
Make rs165815(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19971950
GeneARVCF
is asnp
is mentioned by
dbSNPrs165815
ebirs165815
HLIrs165815
Exacrs165815
Varsomers165815
Maprs165815
PheGenIrs165815
hapmaprs165815
1000 genomesrs165815
hgdprs165815
ensemblrs165815
gopubmedrs165815
geneviewrs165815
scholarrs165815
googlers165815
pharmgkbrs165815
gwascentralrs165815
openSNPrs165815
23andMers165815
23andMe allrs165815
SNP Nexus

SNPshotrs165815
SNPdbers165815
MSV3drs165815
GWAS Ctlgrs165815
GMAF0.3411
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20333729OA-icon.png] A functional variant provided further evidence for the association of ARVCF with schizophrenia


[PMID 15555361] [Searching for a schizophrenia susceptibility gene in the 22q11 region].


[PMID 15861775] Searching for a schizophrenia susceptibility gene in the 22q11 region.


[PMID 18574484OA-icon.png] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.


[PMID 19673036OA-icon.png] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.


GET Evidence
ARVCF-R906Q
aa_change Arg906Gln
aa_change_short R906Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.733036
summary