List of variants in gene PMS2 reported as likely benign for Lynch syndrome 4; Mismatch repair cancer syndrome 4

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.1467G>A (p.Glu489=)	rs542522853	0.00015
NM_000535.7(PMS2):c.1280G>A (p.Arg427His)	rs112902065	0.00007
NM_000535.7(PMS2):c.2043G>A (p.Gln681=)	rs876658953

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