{{Rsnum
|rsid=387906420
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GTF2IRD1
|position=616
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C,G
|CHROM=MT
|CLNACC=RCV000010189.1; RCV000010190.1
|CLNALLE=1; 2
|CLNDBN=Epilepsy, mitochondrial
|CLNHGVS=NC_012920.1:m.616T>C; NC_012920.1:m.616T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590070.0004; 590070.0005
|Disease=Epilepsy
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=616
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906420
}}