List of variants in gene PPARG reported as pathogenic for carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.857G>A (p.Arg286His)	rs28936407	0.00002
NM_138711.6(PPARG):c.466del (p.Ser156fs)	rs587776687
NM_138711.6(PPARG):c.851A>C (p.Gln284Pro)	rs121909242
NM_138711.6(PPARG):c.949A>T (p.Lys317Ter)	rs121909243

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