{{Rsnum
|rsid=2833607
|Chromosome=21
|position=32008727
|Orientation=plus
|GMAF=0.1864
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.4 | 31.0 | 64.6
| HCB | 9.6 | 35.3 | 55.1
| JPT | 4.4 | 37.2 | 58.4
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 7.0 | 93.0
| CHB | 9.6 | 35.3 | 55.1
| CHD | 8.3 | 36.7 | 55.0
| GIH | 4.0 | 37.6 | 58.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 6.9 | 29.3 | 63.8
| MKK | 1.3 | 9.6 | 89.1
| TSI | 5.9 | 41.2 | 52.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19890347
|Trait=Vitiligo
|Title=Genome-Wide Association Study of Generalized Vitiligo in an Isolated European Founder Population Identifies SMOC2, in Close Proximity to IDDM8
|RiskAllele=
|Pval=0.000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2833607
|overall_frequency_n=20
|overall_frequency_d=128
|overall_frequency=0.15625
|n_genomes=16
|n_genomes_annotated=0
|n_haplomes=17
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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