{{Rsnum
|rsid=4743056
|Chromosome=9
|position=97059329
|Orientation=plus
|GMAF=0.494
|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 | 22.1 | 44.2 | 33.6
| HCB | 38.7 | 46.7 | 14.6
| JPT | 41.6 | 48.7 | 9.7
| YRI | 30.6 | 43.5 | 25.9
| ASW | 31.6 | 52.6 | 15.8
| CHB | 38.7 | 46.7 | 14.6
| CHD | 28.4 | 57.8 | 13.8
| GIH | 25.7 | 49.5 | 24.8
| LWK | 20.0 | 49.1 | 30.9
| MEX | 10.3 | 41.4 | 48.3
| MKK | 12.8 | 41.7 | 45.5
| TSI | 25.5 | 46.1 | 28.4
| HapMapRevision=28
}}rs4743056 increases susceptibility to Myasthenia gravis 1.37 times for carriers of the G allele {{PMID|17869649}}

rs4743056 increases susceptibility to Myasthenia gravis, early onset 1.61 times for carriers of the G allele {{PMID|17869649}}

{{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}}