{{Rsnum
|rsid=1054894
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TIMM8A
|position=101346555
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TIMM8A
}}{{omim
|id=300356
|rsnum=1054894
|variant=0007
}}{{ClinVar
|rsid=1054894
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=100601543
|CHROM=X
|dbSNPBuildID=86
|SSR=1
|SAO=1
|VP=0x050260000000070002110100
|GENEINFO=TIMM8A:1678
|GENE_NAME=TIMM8A
|GENE_ID=1678
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.100601543G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300356.0007
|CLNSIG=5
|CLNCUI=C0796074
|CLNDBN=Mohr-Tranebjaerg syndrome
|Disease=Mohr-Tranebjaerg syndrome
|CLNACC=RCV000012076.10
|Tags=RV;PM;S3D;VLD;G5A;G5;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1216:C0796074:304700:52368
}}