{{Rsnum
|rsid=387906423
|Chromosome=MT
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=PYY
|position=8618
|Gene_s=PYY
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=AT
|CHROM=MT
|CLNACC=RCV000010283.3
|CLNALLE=1
|CLNDBN=Neuropathy ataxia retinitis pigmentosa syndrome
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1173:NBK1224:C1838914:551500:644
|CLNHGVS=NC_012920.1:m.8618dupT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516060.0009
|Disease=Neuropathy ataxia retinitis pigmentosa syndrome
|FwdALT=T
|REF=A
|RSPOS=8617
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906423
}}