{{Rsnum
|rsid=6544997
|Chromosome=2
|position=47617366
|Orientation=plus
|GMAF=0.45
|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 | 30.1 | 42.5 | 27.4
| HCB | 35.8 | 44.5 | 19.7
| JPT | 32.7 | 53.1 | 14.2
| YRI | 6.1 | 27.9 | 66.0
| ASW | 5.3 | 36.8 | 57.9
| CHB | 35.8 | 44.5 | 19.7
| CHD | 38.5 | 50.5 | 11.0
| GIH | 25.7 | 39.6 | 34.7
| LWK | 3.6 | 30.0 | 66.4
| MEX | 22.4 | 48.3 | 29.3
| MKK | 2.6 | 45.5 | 51.9
| TSI | 30.7 | 45.5 | 23.8
| 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=0.000007
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6544997
|overall_frequency_n=78
|overall_frequency_d=128
|overall_frequency=0.609375
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=69
|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 | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}