{{Rsnum
|rsid=199476133
|Chromosome=MT
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PYY
|position=8993
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-ATP6
}}{{ClinVar
|ALT=C,G
|CHROM=MT
|CLNACC=RCV000010275.1; RCV000010276.1; RCV000010273.1; RCV000010274.1
|CLNALLE=1; 2
|CLNDBN=Leigh's disease; Ataxia and polyneuropathy, adult-onset; Neuropathy ataxia retinitis pigmentosa syndrome
|CLNDSDB=GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005; C1838916; NBK1173:NBK1224:C1838914:551500:644
|CLNHGVS=NC_012920.1:m.8993T>C; NC_012920.1:m.8993T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516060.0002; 516060.0001
|Disease=Leigh's disease; Ataxia and polyneuropathy; Neuropathy ataxia retinitis pigmentosa syndrome
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=8993
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476133
}}