{{Rsnum
|rsid=397514695
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMEM5
|position=63808778
|Gene_s=TMEM5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000043551.1
|CLNALLE=1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN164735:615041:899
|CLNHGVS=NC_000012.11:g.64202558C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605862.0006
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdALT=T
|FwdREF=C
|GENEINFO=TMEM5:10329
|GENE_ID=10329
|GENE_NAME=TMEM5
|REF=C
|RSPOS=64202558
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514695
}}