ClinVar Miner

List of variants in gene PPARG reported by Personalized Diabetes Medicine Program, University of Maryland School of Medicine

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.913G>C (p.Val305Leu)	rs139894525	0.00135
NM_138711.6(PPARG):c.1295A>G (p.Lys432Arg)	rs756523051	0.00002
NM_138711.6(PPARG):c.832C>T (p.Arg278Cys)	rs1176746892

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