rs1037757

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs1037757(C;G)

Make rs1037757(G;G)

Reference

GRCh38 38.1/142

Chromosome

18

Position

59084822

is a	snp
is	mentioned by
dbSNP	rs1037757
dbSNP (classic)	rs1037757
ClinGen	rs1037757
ebi	rs1037757
HLI	rs1037757
Exac	rs1037757
Gnomad	rs1037757
Varsome	rs1037757
LitVar	rs1037757
Map	rs1037757
PheGenI	rs1037757
Biobank	rs1037757
1000 genomes	rs1037757
hgdp	rs1037757
ensembl	rs1037757
geneview	rs1037757
scholar	rs1037757
google	rs1037757
pharmgkb	rs1037757
gwascentral	rs1037757
openSNP	rs1037757
23andMe	rs1037757
SNPshot	rs1037757
SNPdbe	rs1037757
MSV3d	rs1037757
GWAS Ctlg	rs1037757

GMAF

0.03949

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

GWAS snp
PMID	[PMID 22005931]
Trait
Title	Genome-wide association analysis of age-at-onset in Alzheimer's disease.
Risk Allele
P-val	0.000008
Odds Ratio	None None