List of variants in gene PON2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000305.3(PON2):c.287G>C (p.Arg96Thr)	rs201552995	0.00009
NM_000305.3(PON2):c.677A>G (p.Asn226Ser)	rs200897774	0.00009
NM_000305.3(PON2):c.885G>A (p.Pro295=)	rs778196758	0.00006
NM_000305.3(PON2):c.900G>A (p.Ser300=)	rs191021241	0.00001
NM_000305.3(PON2):c.359T>G (p.Ile120Arg)
NM_000305.3(PON2):c.610GTT[1] (p.Val205del)	rs574854691
NM_000305.3(PON2):c.660T>C (p.Asp220=)
NM_000305.3(PON2):c.75-20dup	rs754815103
NM_000305.3(PON2):c.873C>T (p.Phe291=)

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