ClinVar Miner

List of variants reported as uncertain significance for Lynch syndrome 4 by Division of Medical Genetics, University of Washington

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.1262G>A (p.Arg421Gln)	rs778482303	0.00001
NM_000535.7(PMS2):c.2143C>T (p.His715Tyr)	rs747494931
NM_000535.7(PMS2):c.551T>C (p.Met184Thr)	rs1583387794

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