{{Rsnum
|rsid=7023329
|Gene=MTAP
|Chromosome=9
|position=21816529
|Orientation=plus
|GMAF=0.4752
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MTAP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 26.1 | 49.5 | 24.3
| HCB | 25.5 | 49.6 | 24.8
| JPT | 46.9 | 46.9 | 6.2
| YRI | 20.4 | 49.0 | 30.6
| ASW | 24.6 | 49.1 | 26.3
| CHB | 25.5 | 49.6 | 24.8
| CHD | 21.3 | 49.1 | 29.6
| GIH | 55.4 | 40.6 | 4.0
| LWK | 28.2 | 45.5 | 26.4
| MEX | 33.3 | 49.1 | 17.5
| MKK | 18.1 | 45.8 | 36.1
| TSI | 31.4 | 51.0 | 17.6
| HapMapRevision=28
}}[http://blog.23andme.com/2009/07/06/snpwatch-genetic-variants-near-tumor-suppressor-genes-may-increase-risk-for-brain-and-skin-cancer/ 23andMe blog] [[rs7023329]] A 1.18 [[Melanoma]]

{{PMID Auto GWAS
|PMID=19578364
|Trait=Melanoma
|Title=Genome-wide association study identifies three loci associated with melanoma risk
|RiskAllele=A
|Pval=4E-7
|OR=1.18
|ORtxt=[1.10-1.25]
|OA=1
}}

{{omim
|desc=TYROSINASE; TYR
|id=606933
|rsnum=7023329
}}

{{PMID Auto
|PMID=20574843
|Title=Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
|OA=1
}}

{{omim
|id=155601
|rsnum=7023329
}}

{{omim
|id=601800
|rsnum=7023329
}}

{{omim
|id=613099
|rsnum=7023329
}}

{{PMID Auto
|PMID=22034633
|Title=Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1
}}

{{PMID Auto GWAS
|PMID=21983787
|Trait=None
|Title=Genome-wide association study identifies three new melanoma susceptibility loci.
|RiskAllele=
|Pval=7E-9
|OR=1.2000
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7023329
|overall_frequency_n=64
|overall_frequency_d=128
|overall_frequency=0.5
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=58
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23361049
|Title=Common genetic variants in the 9p21 region and their associations with multiple tumours
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}