ClinVar Miner

List of variants reported as pathogenic for Mismatch repair cancer syndrome 2 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000251.2(MSH2):c.-125_1076+?del
NM_000251.3(MSH2):c.1662-1G>A	rs267607970
NM_000251.3(MSH2):c.2006-5T>A	rs267607990
NM_000251.3(MSH2):c.454del (p.Met152fs)	rs63751449

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