List of variants in gene MSH6 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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.260+265G>A	rs3136231	0.00608
NM_000179.3(MSH6):c.3557-40T>A	rs189436849	0.00587
NM_000179.3(MSH6):c.3172+875A>C	rs187192537	0.00222
NM_000179.3(MSH6):c.261-3611A>G	rs528466684	0.00095
NM_000179.3(MSH6):c.261-565C>T	rs553631780	0.00055
NM_000179.3(MSH6):c.627+267G>A	rs772499816	0.00050
NM_000179.3(MSH6):c.458-509G>A	rs556222101	0.00025
NM_000179.3(MSH6):c.1081C>T (p.Arg361Cys)	rs587782651	0.00012
NM_000179.3(MSH6):c.627+566T>G	rs869312604	0.00011
NM_000179.3(MSH6):c.458-518G>T	rs869312600	0.00009
NM_000179.3(MSH6):c.3801+5G>A	rs201080919	0.00004
NM_000179.3(MSH6):c.1822A>G (p.Ile608Val)	rs201613780	0.00003
NM_000179.3(MSH6):c.3426G>A (p.Thr1142=)	rs747771350	0.00003
NM_000179.3(MSH6):c.2664G>C (p.Lys888Asn)	rs730881798	0.00002
NM_000179.3(MSH6):c.1168G>A (p.Asp390Asn)	rs147737737	0.00001
NM_000179.3(MSH6):c.260+279C>T	rs869312601	0.00001
NM_000179.3(MSH6):c.3300G>A (p.Thr1100=)	rs540252208	0.00001
NM_000179.3(MSH6):c.1021T>G (p.Ser341Ala)	rs1558660119
NM_000179.3(MSH6):c.1207C>A (p.Leu403Ile)	rs876659223
NM_000179.3(MSH6):c.133G>T (p.Gly45Cys)	rs978968846
NM_000179.3(MSH6):c.1400G>A (p.Gly467Asp)	rs1558661547
NM_000179.3(MSH6):c.1904G>A (p.Arg635Lys)	rs1558663439
NM_000179.3(MSH6):c.261-14C>T	rs369366445
NM_000179.3(MSH6):c.3029C>T (p.Thr1010Ile)	rs768925694
NM_000179.3(MSH6):c.3126A>C (p.Lys1042Asn)	rs1558668218
NM_000179.3(MSH6):c.3173-18T>A	rs189672273
NM_000179.3(MSH6):c.3964G>A (p.Glu1322Lys)	rs1553333707
NM_000179.3(MSH6):c.4018A>G (p.Ser1340Gly)	rs1558395603
NM_000179.3(MSH6):c.458-1174T>C	rs869312602
NM_000179.3(MSH6):c.475G>A (p.Ala159Thr)	rs1553411396
NM_000179.3(MSH6):c.511G>C (p.Glu171Gln)	rs1558656518
NM_000179.3(MSH6):c.542A>C (p.Glu181Ala)	rs1558656620
NM_000179.3(MSH6):c.911T>C (p.Val304Ala)	rs1481054050
NM_000179.3(MSH6):c.971A>G (p.Lys324Arg)	rs1558659961

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