rs5355

minus

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

Make rs5355(C;T)

Make rs5355(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169726729

Gene

SELE

is a	snp
is	mentioned by
dbSNP	rs5355
dbSNP (classic)	rs5355
ClinGen	rs5355
ebi	rs5355
HLI	rs5355
Exac	rs5355
Gnomad	rs5355
Varsome	rs5355
LitVar	rs5355
Map	rs5355
PheGenI	rs5355
Biobank	rs5355
1000 genomes	rs5355
hgdp	rs5355
ensembl	rs5355
geneview	rs5355
scholar	rs5355
google	rs5355
pharmgkb	rs5355
gwascentral	rs5355
openSNP	rs5355
23andMe	rs5355
SNPshot	rs5355
SNPdbe	rs5355
MSV3d	rs5355
GWAS Ctlg	rs5355

GMAF

0.03352

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 22589243] Association of E-selectin gene polymorphisms with ischemic stroke in a Chinese Han population

[PMID 16820586 ] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.

[PMID 18513389 ] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

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

[PMID 19330901 ] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

[PMID 19559392 ] A candidate gene association study of 77 polymorphisms in migraine.

[PMID 19619703 ] Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome Study.

[PMID 20031567 ] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.

[PMID 20416077 ] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

[PMID 22815813 ] Functional epistatic interaction between rs6046G>A in F7 and rs5355C>T in SELE modifies systolic blood pressure levels

[PMID 24151105] Association of E-Selectin Gene Polymorphism and Serum PAPP-A with Carotid Atherosclerosis in End-Stage Renal Disease