{{Rsnum
|rsid=1057141
|Gene=TAP1
|Chromosome=6
|position=32850997
|Orientation=minus
|GMAF=0.2034
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TAP1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 76.1 | 21.2 | 2.7
| HCB | 61.8 | 36.8 | 1.5
| JPT | 76.1 | 21.2 | 2.7
| YRI | 54.1 | 40.4 | 5.5
| ASW | 50.9 | 45.6 | 3.5
| CHB | 61.8 | 36.8 | 1.5
| CHD | 66.1 | 27.5 | 6.4
| GIH | 61.4 | 32.7 | 5.9
| LWK | 39.4 | 49.5 | 11.0
| MEX | 63.8 | 32.8 | 3.4
| MKK | 58.1 | 36.1 | 5.8
| TSI | 59.8 | 34.3 | 5.9
| HapMapRevision=28
}}{{omim
|desc=PEPTIDE TRANSPORTER PSF1 POLYMORPHISM
|id=170260
|rsnum=1057141
|variant=0001
}}

{{ClinVar
|rsid=1057141
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=32818774
|CHROM=6
|GMAF=0.2042
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x05017800000017051f110100
|GENEINFO=TAP1:6890
|GENE_NAME=TAP1
|GENE_ID=6890
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32818774T>C
|CLNORIGIN=1
|CLNSIG=2
|Tags=RV;PM;TPA;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.7966; 0.2034
|CLNACC=RCV000014732.1
|CLNDBN=PEPTIDE TRANSPORTER PSF1 POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=170260.0001
|COMMON=1
|Disease=PEPTIDE TRANSPORTER PSF1 POLYMORPHISM
}}

{{PMID Auto
|PMID=12830434
|Title=BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.
|OA=1
}}

{{PMID Auto
|PMID=19387463
|Title=Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC.
|OA=1
}}

{{GET Evidence
|gene=TAP1
|aa_change=Ile393Val
|aa_change_short=I393V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1057141
|overall_frequency_n=1483
|overall_frequency_d=7522
|overall_frequency=0.197155
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=28
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23272491
|Title=[Relationship between rs1057141 and rs1135216 polymorphisms of TAP1 gene and allergic rhinitis in Xinjiang Han people]
}}

{{PMID Auto
|PMID=23395648
|Title=Genetic evidence of TAP1 gene variant as a susceptibility factor in Indian leprosy patients.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | Illumina Human 1M}}