rs10105606

Orientation

plus

Stabilized

plus

Make rs10105606(A;A)

Make rs10105606(A;C)

Make rs10105606(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

19970337

is a	snp
is	mentioned by
dbSNP	rs10105606
dbSNP (classic)	rs10105606
ClinGen	rs10105606
ebi	rs10105606
HLI	rs10105606
Exac	rs10105606
Gnomad	rs10105606
Varsome	rs10105606
LitVar	rs10105606
Map	rs10105606
PheGenI	rs10105606
Biobank	rs10105606
1000 genomes	rs10105606
hgdp	rs10105606
ensembl	rs10105606
geneview	rs10105606
scholar	rs10105606
google	rs10105606
pharmgkb	rs10105606
gwascentral	rs10105606
openSNP	rs10105606
23andMe	rs10105606
SNPshot	rs10105606
SNPdbe	rs10105606
MSV3d	rs10105606
GWAS Ctlg	rs10105606

GMAF

0.3788

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 20864672]
Trait
Title	Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele	C
P-val	4E-26
Odds Ratio	0.07 [0.06-0.08] increase

[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

[PMID 19148283] Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study.

[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.