{{Rsnum
|rsid=11544238
|Gene=ARHGAP9
|Chromosome=12
|position=57476372
|Orientation=minus
|GMAF=0.4151
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ARHGAP9
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 36.6 | 51.8 | 11.6
| HCB | 7.4 | 42.6 | 50.0
| JPT | 26.8 | 50.9 | 22.3
| YRI | 1.4 | 17.0 | 81.6
| ASW | 3.5 | 40.4 | 56.1
| CHB | 7.4 | 42.6 | 50.0
| CHD | 8.3 | 44.0 | 47.7
| GIH | 23.8 | 52.5 | 23.8
| LWK | 4.5 | 30.9 | 64.5
| MEX | 12.1 | 53.4 | 34.5
| MKK | 14.7 | 43.6 | 41.7
| TSI | 43.1 | 46.1 | 10.8
| HapMapRevision=28
}}{{omim
|id=610576
|rsnum=11544238
|variant=0001
}}

{{PMID|19911011}} Mutation of ARHGAP9 in patients with coronary spastic angina.

{{GET Evidence
|gene=ARHGAP9
|aa_change=Ser370Ala
|aa_change_short=S370A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11544238
|overall_frequency_n=5243
|overall_frequency_d=10758
|overall_frequency=0.487358
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|nblosum100=-1
|autoscore=0
|webscore=N
}}

{{ClinVar
|ALT=C
|CAF=0.5849; 0.4151
|CHROM=12
|CLNACC=RCV000001248.4
|CLNALLE=1
|CLNDBN=not provided
|CLNHGVS=NC_000012.11:g.57870155A>C
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610576.0001
|COMMON=1
|Disease=not provided
|FwdALT=G
|FwdREF=T
|GENEINFO=ARHGAP9:64333
|GENE_ID=64333
|GENE_NAME=ARHGAP9
|REF=A
|RSPOS=57870155
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05036800000017051f110100
|WGT=0
|dbSNPBuildID=120
|rsid=11544238
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}