List of variants in gene MSH2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.211+9C>G	rs2303426	0.55454
NM_000251.3(MSH2):c.1759+183G>A	rs3764960	0.42227
NM_000251.3(MSH2):c.1759+107A>G	rs3764959	0.41882
NM_000251.3(MSH2):c.1661+12G>A	rs3732183	0.40290
NM_000251.2(MSH2):c.-118T>C	rs2303425	0.10354
NM_000251.3(MSH2):c.1511-9A>T	rs12998837	0.09123
NM_000251.3(MSH2):c.2006-6T>C	rs2303428	0.08349
NM_000251.3(MSH2):c.380A>G (p.Asn127Ser)	rs17217772	0.02317
NM_000251.3(MSH2):c.573C>T (p.Leu191=)	rs1800151	0.01972
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.1077-10T>C	rs17224360	0.01428
NM_000251.3(MSH2):c.984C>T (p.Ala328=)	rs4987189	0.00495
NM_000251.3(MSH2):c.1666T>C (p.Leu556=)	rs61756466	0.00471
NM_000251.3(MSH2):c.339G>A (p.Lys113=)	rs35898375	0.00313
NM_000251.3(MSH2):c.23C>T (p.Thr8Met)	rs17217716	0.00184
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.942+24_942+29del	rs11309117
NM_000251.3(MSH2):c.942+27_942+29del	rs11309117

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