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rs2235749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2235749(A;A)
Make rs2235749(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position1979293
GeneLOC727993, PDYN
is asnp
is mentioned by
dbSNPrs2235749
dbSNP (classic)rs2235749
ClinGenrs2235749
ebirs2235749
HLIrs2235749
Exacrs2235749
Gnomadrs2235749
Varsomers2235749
LitVarrs2235749
Maprs2235749
PheGenIrs2235749
Biobankrs2235749
1000 genomesrs2235749
hgdprs2235749
ensemblrs2235749
geneviewrs2235749
scholarrs2235749
googlers2235749
pharmgkbrs2235749
gwascentralrs2235749
openSNPrs2235749
23andMers2235749
SNPshotrs2235749
SNPdbers2235749
MSV3drs2235749
GWAS Ctlgrs2235749
GMAF0.4784
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 18923396OA-icon.png] In Caucasians, we found point-wise significant associations of 3' UTR SNPs (rs910080, rs910079, and rs2235749) with cocaine dependence and cocaine/alcohol codependence.



[PMID 21382455] Association between heroin dependence and prodynorphin gene polymorphisms


[PMID 21521424OA-icon.png] Prodynorphin CpG-SNPs associated with alcohol dependence: elevated methylation in the brain of human alcoholics


[PMID 27074815OA-icon.png] A Functional 3'UTR Polymorphism (rs2235749) of Prodynorphin Alters microRNA-365 Binding in Ventral Striatonigral Neurons to Influence Novelty Seeking and Positive Reward Traits


ClinVar
Risk rs2235749(A;A)
Alt rs2235749(A;A)
Reference Rs2235749(G;G)
Significance Non-pathogenic
Disease Spinocerebellar Ataxia
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar Ataxia, Dominant
Reversed 0
HGVS NC_000020.10:g.1959939G>A
CLNSRC
CLNACC RCV000401555.1,