List of variants in gene PPARG reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.1341C>T (p.His447=)	rs3856806	0.11181
NM_138711.6(PPARG):c.248C>A (p.Pro83Gln)	rs1800571	0.00003
NM_138711.6(PPARG):c.857G>A (p.Arg286His)	rs28936407	0.00002
NM_138711.6(PPARG):c.1074T>A (p.Phe358Leu)	rs72551363
NM_138711.6(PPARG):c.1183C>T (p.Arg395Cys)	rs72551364
NM_138711.6(PPARG):c.1394C>T (p.Pro465Leu)	rs121909244
NM_138711.6(PPARG):c.28C>G (p.Pro10Ala)	rs1805192
NM_138711.6(PPARG):c.464_466delinsT (p.Lys155fs)	rs2125215016
NM_138711.6(PPARG):c.466del (p.Ser156fs)	rs587776687
NM_138711.6(PPARG):c.478T>A (p.Cys160Ser)	rs121909245
NM_138711.6(PPARG):c.490C>T (p.Arg164Trp)	rs121909246
NM_138711.6(PPARG):c.851A>C (p.Gln284Pro)	rs121909242
NM_138711.6(PPARG):c.862G>A (p.Val288Met)	rs72551362
NM_138711.6(PPARG):c.949A>T (p.Lys317Ter)	rs121909243

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