{{Rsnum
|rsid=3816873
|Gene=MTTP
|Chromosome=4
|position=99583507
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.2158
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MTTP
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 40.7 | 54.0
| HCB | 0.7 | 19.7 | 79.6
| JPT | 2.7 | 23.9 | 73.5
| YRI | 6.1 | 34.0 | 59.9
| ASW | 5.3 | 40.4 | 54.4
| CHB | 0.7 | 19.7 | 79.6
| CHD | 2.8 | 21.1 | 76.1
| GIH | 15.0 | 37.0 | 48.0
| LWK | 11.0 | 40.4 | 48.6
| MEX | 6.9 | 29.3 | 63.8
| MKK | 14.3 | 46.1 | 39.6
| TSI | 2.9 | 50.0 | 47.1
| HapMapRevision=28
}}Also known as I128T MTP

{{PMID|16721486}} rare allele of the MTP I128T polymorphism may be protective against impaired glucose tolerance, [[type-2 diabetes]]

{{ neighbor
| rsid = 2306986
| distance = 89
}}

{{omim
|id=157147
|desc=MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN, 88-KD; MTP
|rsnum=3816873
}}

{{omim
|id=157147
|rsnum=3816873
|variant=0009
}}

{{ClinVar
|rsid=3816873
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=100504664
|CHROM=4
|GMAF=0.2157
|dbSNPBuildID=107
|SSR=0
|SAO=1
|VP=0x05036800000017051f110100
|GENEINFO=MTTP:4547
|GENE_NAME=MTTP
|GENE_ID=4547
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.100504664T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.7842; 0.2158
|CLNACC=RCV000015310.1
|CLNDBN=Metabolic syndrome, protection against
|CLNDSDB=MedGen
|CLNDSDBID=C1970051
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=157147.0009
|COMMON=1
|Disease=Metabolic syndrome
}}

{{PMID|21438662}} Association of polymorphisms in glutamate-cysteine ligase catalytic subunit and microsomal triglyceride transfer protein genes with nonalcoholic fatty liver disease.

{{GET Evidence
|gene=MTTP
|aa_change=Ile128Thr
|aa_change_short=I128T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3816873
|overall_frequency_n=2862
|overall_frequency_d=10754
|overall_frequency=0.266134
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{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}}