List of variants in gene MSH2 reported as likely pathogenic by Sema4, Sema4

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.1077-1G>C	rs267607944
NM_000251.3(MSH2):c.161_162insGCAGAACGTGGTCGTGG (p.Arg55fs)	rs2103878331
NM_000251.3(MSH2):c.164_165insC (p.Glu56fs)	rs2103878687
NM_000251.3(MSH2):c.170_171insCTACCTCGGCTCGATCCTCGCCGATCCGCGCCCA (p.Phe58fs)	rs2103879195
NM_000251.3(MSH2):c.2635-24A>G	rs1667575488

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