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rs9834692

From SNPedia

Orientationplus
Stabilizedplus
Make rs9834692(C;C)
Make rs9834692(C;T)
Make rs9834692(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87446400
is asnp
is mentioned by
dbSNPrs9834692
ebirs9834692
HLIrs9834692
Exacrs9834692
Varsomers9834692
Maprs9834692
PheGenIrs9834692
hapmaprs9834692
1000 genomesrs9834692
hgdprs9834692
ensemblrs9834692
gopubmedrs9834692
geneviewrs9834692
scholarrs9834692
googlers9834692
pharmgkbrs9834692
gwascentralrs9834692
openSNPrs9834692
23andMers9834692
23andMe allrs9834692
SNP Nexus

SNPshotrs9834692
SNPdbers9834692
MSV3drs9834692
GWAS Ctlgrs9834692
GMAF0.1281
Max Magnitude
? (C;C) (C;T) (T;T) 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