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rs10207628

From SNPedia

Orientationplus
Stabilizedplus
Make rs10207628(C;C)
Make rs10207628(C;G)
Make rs10207628(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127094445
GeneBIN1
is asnp
is mentioned by
dbSNPrs10207628
ebirs10207628
HLIrs10207628
Exacrs10207628
Varsomers10207628
Maprs10207628
PheGenIrs10207628
hapmaprs10207628
1000 genomesrs10207628
hgdprs10207628
ensemblrs10207628
gopubmedrs10207628
geneviewrs10207628
scholarrs10207628
googlers10207628
pharmgkbrs10207628
gwascentralrs10207628
openSNPrs10207628
23andMers10207628
23andMe allrs10207628
SNP Nexus

SNPshotrs10207628
SNPdbers10207628
MSV3drs10207628
GWAS Ctlgrs10207628
GMAF0.1818
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000001
Odds Ratio 1.4100 None