{{Rsnum
|rsid=150736997
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM5
|position=63808776
|Gene_s=TMEM5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=12
|CLNACC=RCV000032804.3
|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.64202556A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605862.0002
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdALT=G
|FwdREF=A
|GENEINFO=TMEM5:10329
|GENE_ID=10329
|GENE_NAME=TMEM5
|REF=A
|RSPOS=64202556
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=150736997
}}