List of variants in gene MSH2 reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

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: 30

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1386+4512G>T	rs75352573	0.01279
NM_000251.3(MSH2):c.1759+1281G>A	rs77300212	0.00719
NM_000251.3(MSH2):c.1276+6958A>T	rs150952868	0.00573
NM_000251.3(MSH2):c.1386+6500A>G	rs76713374	0.00329
NM_000251.3(MSH2):c.2635-320A>G	rs77681063	0.00325
NM_000251.3(MSH2):c.1277-2433T>A	rs186552003	0.00310
NM_000251.3(MSH2):c.1387-6173G>T	rs142227676	0.00255
NM_000251.3(MSH2):c.2635-325C>T	rs116279697	0.00198
NM_000251.3(MSH2):c.1076+4134C>G	rs187772681	0.00196
NM_000251.3(MSH2):c.1077-775C>T	rs17217933	0.00158
NM_000251.3(MSH2):c.2459-312A>G	rs796612837	0.00125
NM_000251.3(MSH2):c.1386+917T>A	rs187069025	0.00108
NM_000251.3(MSH2):c.138C>G (p.His46Gln)	rs33946261	0.00019
NM_000251.3(MSH2):c.4G>A (p.Ala2Thr)	rs63750466	0.00008
NM_000251.3(MSH2):c.1077-766A>G	rs869312596	0.00003
NM_000251.3(MSH2):c.14C>A (p.Pro5Gln)	rs56170584	0.00003
NM_000251.3(MSH2):c.2459-1055A>G	rs553886398	0.00002
NM_000251.3(MSH2):c.1386+149A>T	rs869312599	0.00001
NM_000251.3(MSH2):c.1387-2159A>G	rs869312597	0.00001
NM_000251.3(MSH2):c.763A>G (p.Ser255Gly)	rs761529282	0.00001
NM_000251.3(MSH2):c.12G>T (p.Gln4His)	rs878853800
NM_000251.3(MSH2):c.1386+7642A>G	rs869312598
NM_000251.3(MSH2):c.1387-6187G>A	rs17224514
NM_000251.3(MSH2):c.1850T>C (p.Val617Ala)	rs1260310695
NM_000251.3(MSH2):c.2005+479T>G	rs869312595
NM_000251.3(MSH2):c.2095T>C (p.Ser699Pro)	rs1428704795
NM_000251.3(MSH2):c.2317A>G (p.Lys773Glu)	rs1558521813
NM_000251.3(MSH2):c.2576_2584del (p.Glu859_Gln861del)	rs587781278
NM_000251.3(MSH2):c.271G>C (p.Asp91His)	rs1558457163
NM_000251.3(MSH2):c.896A>G (p.Tyr299Cys)	rs1558464315

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.