{{Rsnum
|rsid=10188217
|Gene=PUS10
|Chromosome=2
|position=60990407
|Orientation=plus
|GMAF=0.4665
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PUS10
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 41.6 | 28.3
| HCB | 0.0 | 8.0 | 92.0
| JPT | 0.0 | 14.2 | 85.8
| YRI | 91.2 | 8.8 | 0.0
| ASW | 73.7 | 26.3 | 0.0
| CHB | 0.0 | 8.0 | 92.0
| CHD | 0.0 | 11.0 | 89.0
| GIH | 7.9 | 34.7 | 57.4
| LWK | 90.9 | 9.1 | 0.0
| MEX | 12.1 | 53.4 | 34.5
| MKK | 78.8 | 19.9 | 1.3
| TSI | 26.5 | 47.1 | 26.5
| HapMapRevision=28
}}[http://blog.23andme.com/2011/02/08/snpwatch-researchers-identify-risk-variants-shared-by-crohn%E2%80%99s-disease-and-celiac-disease/ 23andMe blog] risk factors contributing to both [[celiac disease]] and [[Crohn’s disease]] in nearly 10,000 subjects with either disease and more than 10,000 healthy individuals, all of European ancestry. The CC genotypes at both [[rs10188217]] and [[rs212388]] were associated with slightly higher odds of either disease compared to the CT genotype, and the TT genotypes at both SNPs were associated with slightly lower odds.

{{PMID Auto GWAS
|PMID=21298027
|Trait=None
|Title=A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease
|RiskAllele=C
|Pval=1E-11
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=19068216
|Title=Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
|OA=1
}}

{{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}}