{{Rsnum
|rsid=5355
|Gene=SELE
|Chromosome=1
|position=169726729
|Orientation=minus
|GMAF=0.03352
|Gene_s=SELE
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 95.5 | 4.5 | 0.0
| HCB | 91.0 | 9.0 | 0.0
| JPT | 87.3 | 12.7 | 0.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 91.0 | 9.0 | 0.0
| CHD | 88.0 | 12.0 | 0.0
| GIH | 86.0 | 14.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 96.4 | 3.6 | 0.0
| MKK | 92.3 | 6.4 | 1.3
| TSI | 90.2 | 8.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22589243
|Title=Association of E-selectin gene polymorphisms with ischemic stroke in a Chinese Han population
}}

{{PMID Auto
|PMID=16820586
|Title=Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
|OA=1
}}

{{PMID Auto
|PMID=18513389
|Title=New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
|OA=1
}}

{{PMID Auto
|PMID=19131662
|Title=A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
|OA=1
}}

{{PMID Auto
|PMID=19330901
|Title=Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=19559392
|Title=A candidate gene association study of 77 polymorphisms in migraine.
|OA=1
}}

{{PMID Auto
|PMID=19619703
|Title=Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome Study.
|OA=1
}}

{{PMID Auto
|PMID=20031567
|Title=An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=20416077
|Title=Identification of type 2 diabetes-associated combination of SNPs using support vector machine.
|OA=1
}}

{{GET Evidence
|gene=SELE
|aa_change=Leu575Phe
|aa_change_short=L575F
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs5355
|overall_frequency_n=368
|overall_frequency_d=10758
|overall_frequency=0.0342071
|n_genomes=6
|n_genomes_annotated=0
|n_haplomes=7
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.007
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=22815813
|Title=Functional epistatic interaction between rs6046G&gt;A in F7 and rs5355C&gt;T in SELE modifies systolic blood pressure levels
|OA=1
}}

{{PMID Auto
|PMID=24151105
|Title=Association of E-Selectin Gene Polymorphism and Serum PAPP-A with Carotid Atherosclerosis in End-Stage Renal Disease
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}