{{Rsnum
|rsid=514024
|Gene=SH2D3C
|Chromosome=9
|position=127741791
|Orientation=plus
|GMAF=0.4826
|Gene_s=SH2D3C
|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 | 40.7 | 46.9 | 12.4
| HCB | 7.3 | 41.6 | 51.1
| JPT | 8.8 | 42.5 | 48.7
| YRI | 25.3 | 48.6 | 26.0
| ASW | 35.1 | 49.1 | 15.8
| CHB | 7.3 | 41.6 | 51.1
| CHD | 6.4 | 39.4 | 54.1
| GIH | 31.7 | 58.4 | 9.9
| LWK | 42.7 | 44.5 | 12.7
| MEX | 22.4 | 50.0 | 27.6
| MKK | 35.3 | 50.6 | 14.1
| TSI | 39.2 | 48.0 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23568457
  |Trait=Eating disorders (purging via substances)
  |Title=Genetic variants associated with disordered eating.
  |RiskAllele=A
  |Pval=5E-6
  |OR=.06
  |ORtxt=[0.036-0.086] unit increase
  }}

{{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}}