{{Rsnum
|rsid=2061634
|Gene=C9orf174
|Chromosome=9
|position=97343500
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=G
|GMAF=0.2479
|Gene_s=BDAG1,C9orf174
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 5.3 | 38.1 | 56.6
| HCB | 0.7 | 25.5 | 73.7
| JPT | 2.7 | 24.8 | 72.6
| YRI | 19.2 | 49.3 | 31.5
| ASW | 12.3 | 61.4 | 26.3
| CHB | 0.7 | 25.5 | 73.7
| CHD | 1.8 | 27.5 | 70.6
| GIH | 4.0 | 35.4 | 60.6
| LWK | 13.8 | 52.3 | 33.9
| MEX | 12.3 | 24.6 | 63.2
| MKK | 18.3 | 42.5 | 39.2
| TSI | 5.0 | 35.6 | 59.4
| HapMapRevision=28
}}

{{PMID|19442274|OA=1
}} First genome-wide association study for this disorder, albeit of 152 patients, reports an association between this SNP (odds ratio 2.04, p = 4.2 x10e-5) and [[Behcet's disease]].

{{GET Evidence
|gene=C9ORF174
|aa_change=Ser995Cys
|aa_change_short=S995C
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2061634
|overall_frequency_n=3492
|overall_frequency_d=10758
|overall_frequency=0.324596
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}