{{Rsnum
|rsid = 28936407
|Gene = PPARG
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=12416831
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PPARG
}}NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

{{omim
|desc=COLON CANCER, SOMATIC
|id=601487
|rsnum=28936407
|variant=0006
}}

{{ClinVar
|rsid=28936407
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=12458330
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PPARG:5468
|GENE_NAME=PPARG
|GENE_ID=5468
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.12458330G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000008611.1
|CLNDBN=Colon cancer, somatic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601487.0006
|Disease=Colon cancer
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}