{{Rsnum
|rsid = 28940281
|Gene = ARHGEF10
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=8
|position=1882669
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ARHGEF10
}}{{omim
|desc=SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT
|id=608136
|rsnum=28940281
|variant=0001
}}

{{ClinVar
|rsid=28940281
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=1830835
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ARHGEF10:9639
|GENE_NAME=ARHGEF10
|GENE_ID=9639
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.1830835C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608136.0001
|CLNSIG=5
|CLNCUI=C1842357
|CLNDBN=Slowed nerve conduction velocity, autosomal dominant
|Disease=Slowed nerve conduction velocity
|CLNACC=RCV000002634.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1842357:608236
}}

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