{{Rsnum
|rsid=387907031
|Chromosome=3
|position=119413976
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ARHGAP31
|Gene_s=ARHGAP31
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000023842.1
|CLNALLE=1
|CLNDBN=Adams-Oliver syndrome 1
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN028867:100300:974:34748004
|CLNHGVS=NC_000003.11:g.119132823C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610911.0001
|Disease=Adams-Oliver syndrome 1
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=119132823
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907031
|GENEINFO=ARHGAP31:57514
|GENE_ID=57514
|GENE_NAME=ARHGAP31
}}