ClinVar Miner

List of variants in gene PPARG reported as pathogenic for colonic neoplasm

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_138712.3(PPARG):c.472del (p.Ser158fs) rs587776687
NM_138712.3(PPARG):c.857A>C (p.Gln286Pro) rs121909242
NM_138712.3(PPARG):c.863G>A (p.Arg288His) rs28936407
NM_138712.3(PPARG):c.955A>T (p.Lys319Ter) rs121909243

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