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rs77231105

From SNPedia

Orientationplus
Stabilizedplus
Make rs77231105(A;A)
Make rs77231105(A;G)
Make rs77231105(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position55863084
GeneSEPT14
is asnp
is mentioned by
dbSNPrs77231105
dbSNP (classic)rs77231105
ClinGenrs77231105
ebirs77231105
HLIrs77231105
Exacrs77231105
Gnomadrs77231105
Varsomers77231105
LitVarrs77231105
Maprs77231105
PheGenIrs77231105
Biobankrs77231105
1000 genomesrs77231105
hgdprs77231105
ensemblrs77231105
geneviewrs77231105
scholarrs77231105
googlers77231105
pharmgkbrs77231105
gwascentralrs77231105
openSNPrs77231105
23andMers77231105
SNPshotrs77231105
SNPdbers77231105
MSV3drs77231105
GWAS Ctlgrs77231105
Max Magnitude0

[PMID 27115672] SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.