{{Rsnum
|rsid=121434508
|Gene=TMEM126A
|Chromosome=11
|position=85654139
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TMEM126A
}}{{omim
|id=612988
|rsnum=121434508
|variant=0001
}}{{ClinVar
|rsid=121434508
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=85365183
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=TMEM126A:84233
|GENE_NAME=TMEM126A
|GENE_ID=84233
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.85365183C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612988.0001
|CLNSIG=5
|CLNCUI=C2751812
|CLNDBN=Optic atrophy 7
|Disease=Optic atrophy 7
|CLNACC=RCV000000438.1
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751812:612989:227976
|COMMON=0
}}