{{Rsnum
|rsid=28937880
|Gene=ARFGEF2
|Chromosome=20
|position=48953577
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.004132
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ARFGEF2
}}{{omim
|desc=PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE
|id=605371
|rsnum=28937880
|variant=0001
}}

{{ClinVar
|rsid=28937880
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=47570114
|CHROM=20
|GMAF=0.0041
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=ARFGEF2:10564
|GENE_NAME=ARFGEF2
|GENE_ID=10564
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.47570114G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605371.0001
|CLNSIG=5
|CLNCUI=C1842563
|CLNDBN=Heterotopia, periventricular, autosomal recessive
|Disease=Heterotopia
|CLNACC=RCV000005353.2
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9959; 0.004132
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842563:608097:2149
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}