{{Rsnum
|rsid=121909081
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RAB7A
|position=128807614
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAB7A
}}{{omim
|id=602298
|rsnum=121909081
|variant=0004
}}{{ClinVar
|rsid=121909081
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=128526457
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=RAB7A:7879
|GENE_NAME=RAB7A
|GENE_ID=7879
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.128526457G>C
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=602298.0004; VAR_037887
|CLNSIG=5
|CLNCUI=C1833219
|CLNDBN=Charcot-Marie-Tooth disease type 2B; not provided
|Disease=Charcot-Marie-Tooth disease type 2B; not provided
|CLNACC=RCV000007773.1; RCV000059222.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1285:NBK1358:C1833219:600882:99936
}}{{PMID Auto
|PMID=17060578
|Title=Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.
}}

{{PMID Auto
|PMID=21151572
|Title=Rab7 mutants associated with Charcot-Marie-Tooth disease exhibit enhanced NGF-stimulated signaling.
|OA=1
}}