rs3173798

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs3173798(C;C)

Make rs3173798(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

80656534

Gene

CD36

is a	snp
is	mentioned by
dbSNP	rs3173798
dbSNP (classic)	rs3173798
ClinGen	rs3173798
ebi	rs3173798
HLI	rs3173798
Exac	rs3173798
Gnomad	rs3173798
Varsome	rs3173798
LitVar	rs3173798
Map	rs3173798
PheGenI	rs3173798
Biobank	rs3173798
1000 genomes	rs3173798
hgdp	rs3173798
ensembl	rs3173798
geneview	rs3173798
scholar	rs3173798
google	rs3173798
pharmgkb	rs3173798
gwascentral	rs3173798
openSNP	rs3173798
23andMe	rs3173798
SNPshot	rs3173798
SNPdbe	rs3173798
MSV3d	rs3173798
GWAS Ctlg	rs3173798

GMAF

0.1988

Max Magnitude

0

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

[PMID 23175350] Polymorphism of CD36 gene, carbohydrate metabolism and plasma CD36 concentration in obese children. A preliminary study 

[PMID 18305138] Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol.

[PMID 19403559] Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes.

[PMID 20157514] Positive association of common variants in CD36 with neovascular age-related macular degeneration.

[PMID 22113854] Polymorphism of the CD36 Gene and Cardiovascular Risk Factors in Patients with Coronary Artery Disease Manifested at a Young Age.

[PMID 23856131] Is CD36 gene polymorphism in region encoding lipid-binding domain associated with early onset CAD?

ClinVar
Risk	rs3173798(C;C)
Alt	rs3173798(C;C)
Reference	Rs3173798(T;T)
Significance	Probable-non-pathogenic
Disease	Platelet glycoprotein IV deficiency
Variation	info
Gene	CD36
CLNDBN	Platelet glycoprotein IV deficiency
Reversed	0
HGVS	NC_000007.13:g.80285850T>C
CLNSRC
CLNACC	RCV000350315.1,