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rs1037757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1037757(C;G)
Make rs1037757(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position59084822
is asnp
is mentioned by
dbSNPrs1037757
ebirs1037757
HLIrs1037757
Exacrs1037757
Varsomers1037757
Maprs1037757
PheGenIrs1037757
hapmaprs1037757
1000 genomesrs1037757
hgdprs1037757
ensemblrs1037757
gopubmedrs1037757
geneviewrs1037757
scholarrs1037757
googlers1037757
pharmgkbrs1037757
gwascentralrs1037757
openSNPrs1037757
23andMers1037757
23andMe allrs1037757
SNP Nexus

SNPshotrs1037757
SNPdbers1037757
MSV3drs1037757
GWAS Ctlgrs1037757
GMAF0.03949
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22005931OA-icon.png]
Trait
Title Genome-wide association analysis of age-at-onset in Alzheimer's disease.
Risk Allele
P-val 0.000008
Odds Ratio None None