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rs11981883

From SNPedia

Orientationplus
Stabilizedplus
Make rs11981883(G;G)
Make rs11981883(G;T)
Make rs11981883(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position55824073
GeneSEPT14
is asnp
is mentioned by
dbSNPrs11981883
dbSNP (old)rs11981883
ClinGenrs11981883
ebirs11981883
HLIrs11981883
Exacrs11981883
Gnomadrs11981883
Varsomers11981883
Maprs11981883
PheGenIrs11981883
Biobankrs11981883
1000 genomesrs11981883
hgdprs11981883
ensemblrs11981883
gopubmedrs11981883
geneviewrs11981883
scholarrs11981883
googlers11981883
pharmgkbrs11981883
gwascentralrs11981883
openSNPrs11981883
23andMers11981883
23andMe allrs11981883
SNP Nexus

SNPshotrs11981883
SNPdbers11981883
MSV3drs11981883
GWAS Ctlgrs11981883
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 27115672] SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.