rs10413089

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)		susceptibility to low HDL-cholesterol

Make rs10413089(C;T)

Make rs10413089(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44952331

is a	snp
is	mentioned by
dbSNP	rs10413089
dbSNP (classic)	rs10413089
ClinGen	rs10413089
ebi	rs10413089
HLI	rs10413089
Exac	rs10413089
Gnomad	rs10413089
Varsome	rs10413089
LitVar	rs10413089
Map	rs10413089
PheGenI	rs10413089
Biobank	rs10413089
1000 genomes	rs10413089
hgdp	rs10413089
ensembl	rs10413089
geneview	rs10413089
scholar	rs10413089
google	rs10413089
pharmgkb	rs10413089
gwascentral	rs10413089
openSNP	rs10413089
23andMe	rs10413089
SNPshot	rs10413089
SNPdbe	rs10413089
MSV3d	rs10413089
GWAS Ctlg	rs10413089

GMAF

0.1827

Max Magnitude

0

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

[PMID 20855565] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease

[PMID 21752496] Genetic variation in APOE cluster region and Alzheimer's disease risk.