{{Rsnum
|rsid=397514543
|Chromosome=12
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=TMEM5
|position=63805285
|Gene_s=TMEM5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000032803.2
|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.64199065delG
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605862.0001
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdREF=G
|GENEINFO=TMEM5:10329
|GENE_ID=10329
|GENE_NAME=TMEM5
|REF=AG
|RSPOS=64199064
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397514543
}}