rs2303790

plus

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

Make rs2303790(A;G)

Make rs2303790(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

56983380

Gene

CETP

is a	snp
is	mentioned by
dbSNP	rs2303790
dbSNP (classic)	rs2303790
ClinGen	rs2303790
ebi	rs2303790
HLI	rs2303790
Exac	rs2303790
Gnomad	rs2303790
Varsome	rs2303790
LitVar	rs2303790
Map	rs2303790
PheGenI	rs2303790
Biobank	rs2303790
1000 genomes	rs2303790
hgdp	rs2303790
ensembl	rs2303790
geneview	rs2303790
scholar	rs2303790
google	rs2303790
pharmgkb	rs2303790
gwascentral	rs2303790
openSNP	rs2303790
23andMe	rs2303790
SNPshot	rs2303790
SNPdbe	rs2303790
MSV3d	rs2303790
GWAS Ctlg	rs2303790

GMAF

0.006428

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

OMIM	118470
Desc	CHOLESTEROL ESTER TRANSFER PROTEIN DEFICIENCY
Variant	0002
Related	also

ClinVar
Risk	rs2303790(G;G)
Alt	rs2303790(G;G)
Reference	Rs2303790(A;A)
Significance	Other
Disease	Hyperalphalipoproteinemia
Variation	info
Gene	CETP
CLNDBN	Hyperalphalipoproteinemia
Reversed	0
HGVS	NC_000016.9:g.57017292A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000032602.24,

CETP D442G

[PMID 18560005] Association of cholesteryl ester transfer protein genotypes with CETP mass and activity, lipid levels, and coronary risk.

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

[PMID 19131662 ] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

[PMID 19682379 ] TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population.