{{Rsnum
|rsid=104894500
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAB27A
|position=55224004
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAB27A
}}{{omim
|id=603868
|rsnum=104894500
|variant=0009
}}{{ClinVar
|rsid=104894500
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=55516202
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RAB27A:5873
|GENE_NAME=RAB27A
|GENE_ID=5873
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.55516202G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603868.0009
|CLNSIG=5
|CLNCUI=C1868679
|CLNDBN=Griscelli syndrome type 2
|Disease=Griscelli syndrome type 2
|CLNACC=RCV000006356.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868679:607624:381
}}