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rs11618202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs11618202(G;G)
Make rs11618202(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position30539242
GeneHMGB1
is asnp
is mentioned by
dbSNPrs11618202
dbSNP (classic)rs11618202
ClinGenrs11618202
ebirs11618202
HLIrs11618202
Exacrs11618202
Gnomadrs11618202
Varsomers11618202
LitVarrs11618202
Maprs11618202
PheGenIrs11618202
Biobankrs11618202
1000 genomesrs11618202
hgdprs11618202
ensemblrs11618202
geneviewrs11618202
scholarrs11618202
googlers11618202
pharmgkbrs11618202
gwascentralrs11618202
openSNPrs11618202
23andMers11618202
SNPshotrs11618202
SNPdbers11618202
MSV3drs11618202
GWAS Ctlgrs11618202
GMAF0.06336
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 21116278OA-icon.png]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000007
Odds Ratio 0.0003 [NR] unit decrease (main effect)