{{Rsnum
|rsid=121434310
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RAB3GAP2
|position=220164733
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAB3GAP2
}}{{omim
|id=609275
|rsnum=121434310
|variant=0001
}}{{ClinVar
|rsid=121434310
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=220164733
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=RAB3GAP2:25782
|GENE_NAME=RAB3GAP2
|GENE_ID=25782
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.220164733C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_012414.3:c.3154G>T; 609275.0001
|CLNSIG=5
|CLNCUI=C0796037
|CLNDBN=Martsolf syndrome
|Disease=Martsolf syndrome
|CLNACC=RCV000001894.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796037:212720:ORPHA1387
}}