{{Rsnum
|rsid=145606134
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RAB40AL
|position=102937494
|Gene_s=RAB40AL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=X
|CLNACC=RCV000030692.1
|CLNALLE=1
|CLNDBN=Martin-Probst deafness-mental retardation syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845285:300519:85321
|CLNHGVS=NC_000023.10:g.102192422A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300405.0001
|Disease=Martin-Probst deafness-mental retardation syndrome
|FwdALT=G
|FwdREF=A
|GENEINFO=RAB40AL:282808
|GENE_ID=282808
|GENE_NAME=RAB40AL
|REF=A
|RSPOS=102192422
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000040002110100
|WGT=0
|dbSNPBuildID=134
|rsid=145606134
}}