List of variants reported as uncertain significance for Mismatch repair cancer syndrome 1 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.52A>G (p.Ile18Val)	rs63750123	0.00861
NM_000251.3(MSH2):c.1223A>G (p.Tyr408Cys)	rs63750379	0.00001
NM_000251.3(MSH2):c.942+29del	rs11309117
NM_000535.7(PMS2):c.2186_2187del (p.Leu729fs)	rs587779335

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