List of variants in gene PMS2 reported as uncertain significance for Breast neoplasm

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.1981G>A (p.Glu661Lys)	rs778531080	0.00001
NM_000535.7(PMS2):c.2109G>C (p.Thr703=)	rs775355718
NM_000535.7(PMS2):c.784G>A (p.Ala262Thr)	rs779625900

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