List of variants in gene MSH2 reported as likely benign for carcinoma

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.23C>T (p.Thr8Met)	rs17217716	0.00184
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys)	rs63750006	0.00019
NM_000251.3(MSH2):c.198C>T (p.Tyr66=)	rs730881784	0.00011
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000251.3(MSH2):c.382C>G (p.Leu128Val)	rs145649774	0.00006
NM_000251.3(MSH2):c.817G>A (p.Val273Ile)	rs530814648	0.00003
NM_000251.3(MSH2):c.1200C>G (p.Asn400Lys)	rs1301023135	0.00002
NM_000251.3(MSH2):c.159C>T (p.Ala53=)	rs780178752	0.00001
NM_000251.3(MSH2):c.972G>A (p.Gln324=)	rs63750505	0.00001
NM_000251.3(MSH2):c.1497A>G (p.Ala499=)	rs1357985821
NM_000251.3(MSH2):c.2005+8dup	rs267607992
NM_000251.3(MSH2):c.367-28A>G	rs748645813
NM_000251.3(MSH2):c.741C>A (p.Gly247=)	rs747321505
NM_000251.3(MSH2):c.92C>G (p.Thr31Ser)	rs746635262
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117

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