List of variants reported as likely pathogenic for Lynch syndrome 1 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1905del (p.Ala636fs)	rs2528907310
NM_000251.3(MSH2):c.198del (p.Lys65_Tyr66insTer)	rs2465590422
NM_000251.3(MSH2):c.2211-2A>C	rs267608001
NM_000251.3(MSH2):c.802_803insGT (p.Ser268fs)	rs2465780424

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