{{Rsnum
|rsid=199476135
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PYY
|position=9176
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-ATP6
}}{{ClinVar
|ALT=C,G
|CHROM=MT
|CLNACC=RCV000010278.1; RCV000010279.1; RCV000010285.1
|CLNALLE=1; 2
|CLNDBN=Striatonigral degeneration, infantile, mitochondrial; Leigh's disease
|CLNDSDB=MedGen:OMIM; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1839022:500003; NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005
|CLNHGVS=NC_012920.1:m.9176T>C; NC_012920.1:m.9176T>G
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500595; 516060.0005; 516060.0011
|Disease=Striatonigral degeneration; Leigh's disease
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=9176
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476135
}}