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rs7687945

From SNPedia

Orientationplus
Stabilizedplus
Make rs7687945(C;C)
Make rs7687945(C;T)
Make rs7687945(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position89843548
is asnp
is mentioned by
dbSNPrs7687945
ebirs7687945
HLIrs7687945
Exacrs7687945
Varsomers7687945
Maprs7687945
PheGenIrs7687945
hapmaprs7687945
1000 genomesrs7687945
hgdprs7687945
ensemblrs7687945
gopubmedrs7687945
geneviewrs7687945
scholarrs7687945
googlers7687945
pharmgkbrs7687945
gwascentralrs7687945
openSNPrs7687945
23andMers7687945
23andMe allrs7687945
SNP Nexus

SNPshotrs7687945
SNPdbers7687945
MSV3drs7687945
GWAS Ctlgrs7687945
Max Magnitude
? (C;C) (C;T) (T;T) 28
"Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21" [PMID 21044948OA-icon.png] suggests this is Parkinson's Disease associated together with rs356220, masked in other GWAS by rs2736990 via Simpson's paradox. Association replicated in French dataset with r^2 0.98 LD rs2301134 substituted.