List of variants in gene PPARG reported as uncertain significance for overnutrition

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.348T>C (p.Ala116=)	rs147975759	0.00056
NM_138711.6(PPARG):c.391-3C>T	rs370830238	0.00017
NM_138711.6(PPARG):c.417G>A (p.Leu139=)	rs41415646	0.00015
NM_138711.6(PPARG):c.198C>T (p.Asp66=)	rs753817211	0.00004
NM_138711.6(PPARG):c.1224A>G (p.Gln408=)	rs28763894	0.00003
NM_138711.6(PPARG):c.145G>A (p.Glu49Lys)	rs777334819	0.00002
NM_138711.6(PPARG):c.393T>C (p.Gly131=)	rs201126401	0.00002
NM_138711.6(PPARG):c.1116C>A (p.Phe372Leu)	rs886057902
NM_138711.6(PPARG):c.1419C>T (p.Asp473=)	rs886057903
NM_138711.6(PPARG):c.431A>G (p.Asp144Gly)	rs1211829538
NM_138711.6(PPARG):c.56A>C (p.Asp19Ala)	rs762280243
NM_138711.6(PPARG):c.78C>G (p.His26Gln)

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