{{Rsnum
|rsid=199476120
|Gene=ANKRD20A19P
|Chromosome=MT
|position=3397
|Orientation=plus
|GMAF=0.0009355
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MT-ND1
}}{{ClinVar
|ALT=G
|CAF=0.9991; 0.0009355
|CHROM=MT
|CLNACC=RCV000010376.2; RCV000010377.1
|CLNALLE=1
|CLNDBN=Alzheimer's disease; Parkinson's disease
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1161:NBK1236:C0002395:104300:1020:26929004; NBK1208:NBK1223:C0030567:168600:49049000
|CLNHGVS=NC_012920.1:m.3397A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0005
|COMMON=0
|Disease=Alzheimer's disease; Parkinson's disease
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=3397
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476120
}}