List of variants in gene MSH2 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.211+9C>G	rs2303426	0.55454
NM_000251.3(MSH2):c.1077-80G>A	rs2347794	0.53152
NM_000251.3(MSH2):c.1661+12G>A	rs3732183	0.40290
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.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.1077-10T>C	rs17224360	0.01428
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.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.815C>T (p.Ala272Val)	rs34136999	0.00046
NM_000251.3(MSH2):c.1680T>C (p.Asn560=)	rs200056411	0.00043
NM_000251.3(MSH2):c.1886A>G (p.Gln629Arg)	rs61756468	0.00042
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.471C>A (p.Gly157=)	rs61756463	0.00029
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys)	rs63750006	0.00019
NM_000251.3(MSH2):c.1730T>C (p.Ile577Thr)	rs63749910	0.00018
NM_000251.3(MSH2):c.1275A>G (p.Glu425=)	rs63751650	0.00016
NM_000251.3(MSH2):c.2425G>A (p.Glu809Lys)	rs202145681	0.00013
NM_000251.3(MSH2):c.505A>G (p.Ile169Val)	rs63750716	0.00013
NM_000251.3(MSH2):c.2210+7G>T	rs374675118	0.00010
NM_000251.3(MSH2):c.1690A>G (p.Thr564Ala)	rs55778204	0.00008
NM_000251.3(MSH2):c.499G>C (p.Asp167His)	rs63750255	0.00006
NM_000251.3(MSH2):c.1963G>A (p.Val655Ile)	rs549467183	0.00003
NM_000251.3(MSH2):c.2120G>A (p.Cys707Tyr)	rs373226409	0.00003
NM_000251.3(MSH2):c.2205C>T (p.Ile735=)	rs533553381	0.00003
NM_000251.3(MSH2):c.942+5A>G	rs769242733	0.00001
NM_000251.3(MSH2):c.972G>A (p.Gln324=)	rs63750505	0.00001
NM_000251.3(MSH2):c.1387-14_1387-11del	rs370436680
NM_000251.3(MSH2):c.273TCT[2] (p.Leu94del)	rs267607919
NM_000251.3(MSH2):c.67T>C (p.Phe23Leu)	rs372619120
NM_000251.3(MSH2):c.942+29del	rs11309117

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