{{Rsnum
|rsid=9657362
|Gene=ARHGEF10
|Chromosome=8
|position=1885635
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.1359
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ARHGEF10
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 1.6 | 28.6 | 69.8
| HCB | 4.5 | 36.4 | 59.1
| JPT | 11.9 | 31.0 | 57.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.5 | 36.4 | 59.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=9657362
|allele=C
|frequency=
|uid=1103652214412
|type=heterozygous_SNP
|hugo=ARHGEF10
|ensembl gene=ENSG00000104728
|ensembl transcript=ENST00000349830
|sift=TOLERATED
|disease=Defects in ARHGEF10 are the cause of slowed nerve conduction velocity (SNCV) (MIM:608236). Affected individuals present a reduction in nerve conduction velocities without any clinical signs of peripheral or central nervous system dysfunction. SNCV inheritance is autosomal dominant.
}}

{{GET Evidence
|gene=ARHGEF10
|aa_change=Leu370Phe
|aa_change_short=L370F
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9657362
|overall_frequency_n=1151
|overall_frequency_d=10758
|overall_frequency=0.10699
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}