List of variants in gene PPARG reported as likely benign 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: 6

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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.-8-28078C>G	rs1801282	0.08816
NM_138711.6(PPARG):c.1281A>G (p.Ser427=)	rs41516544	0.00627
NM_138711.6(PPARG):c.1362C>T (p.Ile454=)	rs149367249	0.00250
NM_138711.6(PPARG):c.150C>T (p.Asp50=)	rs112174008	0.00154
NM_138711.6(PPARG):c.-8-28133C>T	rs200479885	0.00001

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