rs10743430

Orientation

plus

Stabilized

plus

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

Make rs10743430(C;C)

Make rs10743430(C;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

21998639

is a	snp
is	mentioned by
dbSNP	rs10743430
dbSNP (classic)	rs10743430
ClinGen	rs10743430
ebi	rs10743430
HLI	rs10743430
Exac	rs10743430
Gnomad	rs10743430
Varsome	rs10743430
LitVar	rs10743430
Map	rs10743430
PheGenI	rs10743430
Biobank	rs10743430
1000 genomes	rs10743430
hgdp	rs10743430
ensembl	rs10743430
geneview	rs10743430
scholar	rs10743430
google	rs10743430
pharmgkb	rs10743430
gwascentral	rs10743430
openSNP	rs10743430
23andMe	rs10743430
SNPshot	rs10743430
SNPdbe	rs10743430
MSV3d	rs10743430
GWAS Ctlg	rs10743430

GMAF

0.191

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21116278]
Trait
Title	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val	6E-7
Odds Ratio	0.2181 [NR] unit decrease (main effect)