{{Rsnum
|rsid=6133
|Gene=SELP
|Chromosome=1
|position=169596108
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.1993
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=SELP
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 78.6 | 19.6 | 1.8
| HCB | 98.5 | 1.5 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 11.6 | 46.9 | 41.5
| ASW | 24.6 | 52.6 | 22.8
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 13.6 | 44.5 | 41.8
| MEX | 79.3 | 20.7 | 0.0
| MKK | 20.8 | 53.9 | 25.3
| TSI | 78.2 | 18.8 | 3.0
| HapMapRevision=28
}}{{omim
|desc=ATOPY, SUSCEPTIBILITY TO
|id=173610
|rsnum=6133
|variant=0002
}}

{{PMID Auto
|PMID=19404301
|Title=Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE
|OA=1
}}

{{PMID Auto
|PMID=19240957
|Title=Candidate gene analysis of selectin cluster in patients with multiple sclerosis
}}

{{ClinVar
|rsid=6133
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=169596108
|CHROM=1
|GMAF=0.2001
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x050168000a1515051f110100
|GENEINFO=SELP:6403
|GENE_NAME=SELP
|GENE_ID=6403
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000001.11:g.169596108C>G
|CLNORIGIN=1
|CLNSRCID=
NM_003005.3:c.1918G>C; 173610.0002
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000014483.1
|Tags=RV;PM;PMC;SLO;NSM;REF;OTH;ASP;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.8007; 0.1993; .
|CLNDBN=Atopy, susceptibility to
|CLNDSDB=MedGen
|CLNDSDBID=C1840254
|CLNSRC=ClinVar; OMIM Allelic Variant
|COMMON=1
|Disease=Atopy
}}

{{PMID Auto
|PMID=15726497
|Title=Gene-environment interaction effects on the development of immune responses in the 1st year of life.
|OA=1
}}

{{PMID Auto
|PMID=16820586
|Title=Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
|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=19263529
|Title=Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
|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
}}

{{GET Evidence
|gene=SELP
|aa_change=Val640Leu
|aa_change_short=V640L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6133
|overall_frequency_n=2901
|overall_frequency_d=10758
|overall_frequency=0.26966
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|qualitycomment_in_silico=Y
|in_omim=Y
|nblosum100=0
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=24504449
|Title=SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis
}}

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