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rs16997087

From SNPedia

Orientationplus
Stabilizedplus
Make rs16997087(C;C)
Make rs16997087(C;T)
Make rs16997087(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position16074337
is asnp
is mentioned by
dbSNPrs16997087
ebirs16997087
HLIrs16997087
Exacrs16997087
Varsomers16997087
Maprs16997087
PheGenIrs16997087
hapmaprs16997087
1000 genomesrs16997087
hgdprs16997087
ensemblrs16997087
gopubmedrs16997087
geneviewrs16997087
scholarrs16997087
googlers16997087
pharmgkbrs16997087
gwascentralrs16997087
openSNPrs16997087
23andMers16997087
23andMe allrs16997087
SNP Nexus

SNPshotrs16997087
SNPdbers16997087
MSV3drs16997087
GWAS Ctlgrs16997087
GMAF0.06244
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 1E-10
Odds Ratio NR NR