{{Rsnum
|rsid=1343879
|Gene=MAGEE2
|Chromosome=X
|position=75784694
|Orientation=plus
|GMAF=0.2975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MAGEE2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 1.8 | 0.9 | 97.3
| HCB | 86.8 | 11.0 | 2.2
| JPT | 93.8 | 5.4 | 0.9
| YRI | 0.7 | 0.7 | 98.6
| ASW | 8.9 | 7.1 | 83.9
| CHB | 86.8 | 11.0 | 2.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 20.8 | 14.9 | 64.4
| LWK | 2.7 | 3.6 | 93.6
| MEX | 24.6 | 17.5 | 57.9
| MKK | 0.6 | 1.9 | 97.4
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{omim
|desc=MELANOMA ANTIGEN, FAMILY E, 2; MAGEE2
|id=300760
|rsnum=1343879
}}

{{PMID|19200524|OA=1
}} A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.

{{GET Evidence
|gene=MAGEE2
|aa_change=Glu120Stop
|aa_change_short=E120X
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1343879
|overall_frequency_n=263
|overall_frequency_d=8761
|overall_frequency=0.0300194
|n_genomes=12
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|nblosum100=10
|autoscore=2
|webscore=N
}}

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