List of variants in gene MSH2 reported as likely pathogenic by Department of Molecular Diagnostics, Institute of Oncology Ljubljana

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1015C>T (p.Gln339Ter)	rs1558466577
NM_000251.3(MSH2):c.1661G>A (p.Ser554Asn)	rs63750597
NM_000251.3(MSH2):c.1763_1764del (p.Tyr588fs)	rs1667229261
NM_000251.3(MSH2):c.561_569del (p.Glu188_Leu190del)	rs63750088
NM_000251.3(MSH2):c.942+1del	rs1194793421

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