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rs910079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs910079(A;G)
Make rs910079(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position1979552
GeneLOC727993, PDYN
is asnp
is mentioned by
dbSNPrs910079
dbSNP (old)rs910079
ClinGenrs910079
ebirs910079
HLIrs910079
Exacrs910079
Gnomadrs910079
Varsomers910079
Maprs910079
PheGenIrs910079
Biobankrs910079
1000 genomesrs910079
hgdprs910079
ensemblrs910079
gopubmedrs910079
geneviewrs910079
scholarrs910079
googlers910079
pharmgkbrs910079
gwascentralrs910079
openSNPrs910079
23andMers910079
23andMe allrs910079
SNP Nexus

SNPshotrs910079
SNPdbers910079
MSV3drs910079
GWAS Ctlgrs910079
GMAF0.4789
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.
Neighborrs2235749
Distance259
Neighborrs910080
Distance28
[PMID 19155191OA-icon.png] Opiate and cocaine addiction: from bench to clinic and back to the bench.


ClinVar
Risk rs910079(C;C) rs910079(G;G)
Alt rs910079(C;C) rs910079(G;G)
Reference Rs910079(A;A)
Significance Non-pathogenic
Disease Spinocerebellar Ataxia
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar Ataxia, Dominant
Reversed 0
HGVS NC_000020.10:g.1960198A>G
CLNSRC
CLNACC RCV000353637.1,