{{Rsnum
|rsid=137853052
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAB3GAP1
|position=135150456
|Gene_s=RAB3GAP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602536
|variant=0004
|rsnum=137853052
}}{{ClinVar
|rsid=137853052
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=135908026
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RAB3GAP1:22930
|GENE_NAME=RAB3GAP1
|GENE_ID=22930
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.135908026C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602536.0004
|CLNSIG=5
|CLNCUI=C1838625
|CLNDBN=Warburg micro syndrome 1
|Disease=Warburg micro syndrome 1
|CLNACC=RCV000007475.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1838625:600118:2510
}}