{{Rsnum
|rsid=1801334
|Gene=PARK2
|Chromosome=6
|position=161360193
|Orientation=plus
|GMAF=0.02066
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PARK2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 10.6 | 89.4
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 1.7 | 98.3
| MKK | 0.0 | 0.6 | 99.4
| TSI | 0.0 | 3.9 | 96.1
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1801334
|allele=T
|frequency=
|uid=1103705057970
|type=heterozygous_SNP
|hugo=PARK2
|ensembl gene=ENSG00000185345
|ensembl transcript=ENST00000366898
|sift=AFFECT FUNCTION
|disease=Defects in PARK2 may be involved in the development and/or progression of ovarian cancer.
}}

{{PMID Auto
|PMID=12975291
|Title=Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
}}

{{PMID Auto
|PMID=16269266
|Title=Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease.
}}

{{ClinVar
|rsid=1801334
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=161781225
|CHROM=6
|GMAF=0.0206
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x05016800000015051f100100
|GENEINFO=PARK2:5071
|GENE_NAME=PARK2
|GENE_ID=5071
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.161781225C>T
|CLNORIGIN=0
|CLNSIG=2
|Tags=RV;PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.9793; 0.02066
|CLNACC=RCV000034121.2
|CLNDBN=Parkinson disease 2
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1223:NBK1478:C1868675:600116:2828
|CLNSRC=GeneReviews
|CLNSRCID=NBK1478
|COMMON=1
|Disease=Parkinson disease 2
}}

{{GET Evidence
|gene=PARK2
|aa_change=Asp394Asn
|aa_change_short=D394N
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1801334
|overall_frequency_n=343
|overall_frequency_d=10758
|overall_frequency=0.0318832
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.004
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-1
|autoscore=3
|n_web_uneval=5
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}