{{Rsnum
|rsid = 28933402
|Gene = SURF1
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=9
|position=133353893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SURF1
}}{{omim
|desc=LEIGH SYNDROME DUE TO CYTOCHROME c OXIDASE DEFICIENCY
|id=185620
|rsnum=28933402
|variant=0012
}}

[[Leigh syndrome]] is more common in some [[French-Canadian]] populations. {{PMID|12529507|OA=1
}}

{{ClinVar
|rsid=28933402
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=136220748
|CHROM=9
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000000402110100
|GENEINFO=SURF1:6834
|GENE_NAME=SURF1
|GENE_ID=6834
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.136220748C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=185620.0012
|CLNSIG=5
|CLNCUI=C1850599; C1850599
|CLNDBN=Congenital myasthenic syndrome, acetazolamide-responsive
|Disease=Congenital myasthenic syndrome
|CLNACC=RCV000013606.16
|Tags=RV;PM;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850599:614198:590
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}