List of variants in gene MSH2 reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1277-8T>C	rs145400590	0.00159
NM_000251.3(MSH2):c.1387-8G>T	rs187525243	0.00143
NM_000251.3(MSH2):c.1737A>G (p.Lys579=)	rs61756467	0.00138
NM_000251.3(MSH2):c.819A>G (p.Val273=)	rs146577635	0.00101
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=)	rs63750330	0.00053
NM_000251.3(MSH2):c.1680T>C (p.Asn560=)	rs200056411	0.00043
NM_000251.3(MSH2):c.1168C>T (p.Leu390Phe)	rs17224367	0.00039
NM_000251.3(MSH2):c.2154A>G (p.Gln718=)	rs63750810	0.00033
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser)	rs41295288	0.00022
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys)	rs63750006	0.00019
NM_000251.3(MSH2):c.138C>G (p.His46Gln)	rs33946261	0.00019
NM_000251.3(MSH2):c.505A>G (p.Ile169Val)	rs63750716	0.00013
NM_000251.3(MSH2):c.198C>T (p.Tyr66=)	rs730881784	0.00011
NM_000251.3(MSH2):c.2271C>T (p.Tyr757=)	rs56076152	0.00006
NM_000251.3(MSH2):c.2458+8C>G	rs189025757	0.00003
NM_000251.3(MSH2):c.2061C>G (p.Leu687=)	rs63750032	0.00002
NM_000251.3(MSH2):c.1194A>G (p.Ala398=)	rs1060504412	0.00001
NM_000251.3(MSH2):c.1759+9A>C	rs994093288	0.00001

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