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rs9883474

From SNPedia

Orientationplus
Stabilizedplus
Make rs9883474(A;A)
Make rs9883474(A;C)
Make rs9883474(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position87476299
is asnp
is mentioned by
dbSNPrs9883474
ClinGenrs9883474
ebirs9883474
HLIrs9883474
Exacrs9883474
Varsomers9883474
Maprs9883474
PheGenIrs9883474
hapmaprs9883474
1000 genomesrs9883474
hgdprs9883474
ensemblrs9883474
gopubmedrs9883474
geneviewrs9883474
scholarrs9883474
googlers9883474
pharmgkbrs9883474
gwascentralrs9883474
openSNPrs9883474
23andMers9883474
23andMe allrs9883474
SNP Nexus

SNPshotrs9883474
SNPdbers9883474
MSV3drs9883474
GWAS Ctlgrs9883474
GMAF0.1492
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23471985OA-icon.png]
Trait Brain connectivity
Title Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.
Risk Allele
P-val 3E-9
Odds Ratio NR NR