{{Rsnum
|rsid=199476136
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PYY
|position=8851
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-ATP6
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010280.3
|CLNALLE=1
|CLNDBN=Striatonigral degeneration, infantile, mitochondrial
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1839022:500003
|CLNHGVS=NC_012920.1:m.8851T>C
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500595; 516060.0006
|Disease=Striatonigral degeneration
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=8851
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476136
}}