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

rs1941184

From SNPedia

Orientationminus
Stabilizedminus
Make rs1941184(G;G)
Make rs1941184(G;T)
Make rs1941184(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31458160
GeneDSG3
is asnp
is mentioned by
dbSNPrs1941184
ebirs1941184
HLIrs1941184
Exacrs1941184
Varsomers1941184
Maprs1941184
PheGenIrs1941184
hapmaprs1941184
1000 genomesrs1941184
hgdprs1941184
ensemblrs1941184
gopubmedrs1941184
geneviewrs1941184
scholarrs1941184
googlers1941184
pharmgkbrs1941184
gwascentralrs1941184
openSNPrs1941184
23andMers1941184
23andMe allrs1941184
SNP Nexus

SNPshotrs1941184
SNPdbers1941184
MSV3drs1941184
GWAS Ctlgrs1941184
GMAF0.3678
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19772629OA-icon.png]
Trait Parkinson disease (age of onset)
Title Genomewide Association Study for Onset Age in Parkinson Disease
Risk Allele C
P-val 0.000004
Odds Ratio 2.28 [NR] years younger


GET Evidence
rs1941184
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.404762
summary