List of variants in gene MSH2 reported as uncertain significance for mismatch repair cancer syndrome 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser)	rs41295288	0.00022
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser)	rs201118107	0.00014
NM_000251.3(MSH2):c.128A>G (p.Tyr43Cys)	rs17217723	0.00011
NM_000251.3(MSH2):c.1217G>A (p.Arg406Gln)	rs146567853	0.00008
NM_000251.3(MSH2):c.1045C>G (p.Pro349Ala)	rs267607939	0.00007
NM_000251.3(MSH2):c.1238A>C (p.Gln413Pro)	rs587779962	0.00004
NM_000251.3(MSH2):c.2516A>G (p.His839Arg)	rs63750027	0.00004
NM_000251.3(MSH2):c.1963G>A (p.Val655Ile)	rs549467183	0.00003
NM_000251.3(MSH2):c.1681G>A (p.Glu561Lys)	rs63750328	0.00002
NM_000251.3(MSH2):c.2009C>T (p.Pro670Leu)	rs41294982	0.00002
NM_000251.3(MSH2):c.2379G>T (p.Gln793His)	rs767520406	0.00002
NM_000251.3(MSH2):c.1223A>G (p.Tyr408Cys)	rs63750379	0.00001
NM_000251.3(MSH2):c.1254A>G (p.Ile418Met)	rs751431238	0.00001
NM_000251.3(MSH2):c.1802A>G (p.Gln601Arg)	rs779447213	0.00001
NM_000251.3(MSH2):c.1825G>T (p.Ala609Ser)	rs150980616	0.00001
NM_000251.3(MSH2):c.1927G>A (p.Glu643Lys)	rs374840361	0.00001
NM_000251.3(MSH2):c.274C>G (p.Leu92Val)	rs587779154	0.00001
NM_000251.3(MSH2):c.376G>A (p.Gly126Ser)	rs767371843	0.00001
NM_000251.3(MSH2):c.383T>G (p.Leu128Arg)	rs730881768
NM_000251.3(MSH2):c.403C>G (p.Leu135Val)	rs193096019
NM_000251.3(MSH2):c.464T>C (p.Val155Ala)	rs876658188
NM_000251.3(MSH2):c.942+29del	rs11309117

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