List of variants in gene MSH6 reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.261-36A>G	rs1800931	0.03614
NM_000179.3(MSH6):c.2253T>C (p.Asn751=)	rs2020913	0.02003
NM_000179.3(MSH6):c.1164C>T (p.His388=)	rs55708305	0.01384
NM_000179.3(MSH6):c.2272C>T (p.Leu758=)	rs56371757	0.01363
NM_000179.3(MSH6):c.3306T>A (p.Thr1102=)	rs2020910	0.00869
NM_000179.3(MSH6):c.3557-40T>A	rs189436849	0.00587
NM_000179.3(MSH6):c.1186C>G (p.Leu396Val)	rs2020908	0.00565
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.457+13A>G	rs1800933	0.00434
NM_000179.3(MSH6):c.3439-16C>T	rs192614006	0.00237
NM_000179.3(MSH6):c.431G>T (p.Ser144Ile)	rs3211299	0.00158
NM_000179.3(MSH6):c.3647-6T>A	rs182871847	0.00134
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.3557-3A>T	rs41295274	0.00004
NM_000179.3(MSH6):c.3151G>A (p.Val1051Ile)	rs576269342
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3557-4del	rs267608102
NM_000179.3(MSH6):c.3557-4dup	rs267608102
NM_000179.3(MSH6):c.3557-5_3557-4del
NM_000179.3(MSH6):c.3557-5_3557-4dup	rs267608102
NM_000179.3(MSH6):c.4001+42_4001+46dup
NM_000179.3(MSH6):c.4001+50_4001+51dup	rs199687113
NM_000179.3(MSH6):c.4002-11_4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-12_4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-13_4002-10del
NM_000179.3(MSH6):c.4002-14_4002-10del
NM_000179.3(MSH6):c.4002-26_4002-25insCTTT	rs1553333916
NM_000179.3(MSH6):c.457+32TG[10]	rs397839804

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