{{Rsnum
|rsid=6477872
|Gene=TCEA1P1
|Chromosome=9
|position=97069874
|Orientation=plus
|GMAF=0.174
|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 | 13.3 | 38.1 | 48.7
| HCB | 0.0 | 2.9 | 97.1
| JPT | 0.0 | 1.8 | 98.2
| YRI | 2.0 | 19.7 | 78.2
| ASW | 3.6 | 21.4 | 75.0
| CHB | 0.0 | 2.9 | 97.1
| CHD | 0.0 | 4.6 | 95.4
| GIH | 5.9 | 28.7 | 65.3
| LWK | 5.5 | 16.5 | 78.0
| MEX | 0.0 | 34.5 | 65.5
| MKK | 3.2 | 26.3 | 70.5
| TSI | 11.8 | 45.1 | 43.1
| HapMapRevision=28
}}{{Report GE
|PubMed=17869649
|Source=pubmed
|AffyProbeset=SNP_A-2014384
|AffyOrientation=same
|AlleleA=C
|AlleleB=T
|onGW5=
|rsid=6477872
|ancestral=T
|RiskPopulation=German
|RiskAllele=C
|CaseFreq=0.38
|ControlFreq=0.31
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.38
|Disease=Myasthenia gravis
|DiseaseSymbol=MG
}}

rs6477872 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myasthenia gravis 1.38 times for carriers of the C allele {{PMID|17869649}}

rs6477872 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myasthenia gravis, early onset 1.82 times for carriers of the C allele {{PMID|17869649}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}