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rs10241628

From SNPedia

Orientationplus
Make rs10241628(A;A)
Make rs10241628(A;G)
Make rs10241628(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position55877867
is asnp
is mentioned by
dbSNPrs10241628
ebirs10241628
HLIrs10241628
Exacrs10241628
Varsomers10241628
Maprs10241628
PheGenIrs10241628
hapmaprs10241628
1000 genomesrs10241628
hgdprs10241628
ensemblrs10241628
gopubmedrs10241628
geneviewrs10241628
scholarrs10241628
googlers10241628
pharmgkbrs10241628
gwascentralrs10241628
openSNPrs10241628
23andMers10241628
23andMe allrs10241628
SNP Nexus

SNPshotrs10241628
SNPdbers10241628
MSV3drs10241628
GWAS Ctlgrs10241628
Max Magnitude
? (A;A) (A;G) (G;G) 28

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