List of variants in gene MYH6 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.1275C>T (p.Ile425=)	rs61742470	0.00232
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala)	rs142992009	0.00153
NM_002471.4(MYH6):c.3979-15C>A	rs529249069	0.00146
NM_002471.4(MYH6):c.3979-7T>G	rs535111647	0.00142
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser)	rs143978652	0.00110
NM_002471.4(MYH6):c.2430-14C>T	rs190342289	0.00108
NM_002471.4(MYH6):c.1083G>T (p.Gly361=)	rs138928022	0.00092
NM_002471.4(MYH6):c.5601G>A (p.Gln1867=)	rs148984154	0.00062
NM_002471.4(MYH6):c.643-5C>T	rs199859986	0.00041
NM_002471.4(MYH6):c.4611G>A (p.Val1537=)	rs142983918	0.00030
NM_002471.4(MYH6):c.4293G>A (p.Met1431Ile)	rs201016285	0.00029
NM_002471.4(MYH6):c.5410C>A (p.Gln1804Lys)	rs144571463	0.00029
NM_002471.4(MYH6):c.981C>T (p.Ser327=)	rs148407931	0.00029
NM_002471.4(MYH6):c.2685+10C>T	rs202155137	0.00024
NM_002471.4(MYH6):c.4359+10G>A	rs368183862	0.00024
NM_002471.4(MYH6):c.4137G>A (p.Thr1379=)	rs372158844	0.00022
NM_002471.4(MYH6):c.4505G>A (p.Arg1502Gln)	rs199936506	0.00022
NM_002471.4(MYH6):c.2841C>T (p.Asp947=)	rs140305424	0.00019
NM_002471.4(MYH6):c.824T>A (p.Ile275Asn)	rs201327273	0.00019
NM_002471.4(MYH6):c.3894G>A (p.Ala1298=)	rs151135141	0.00016
NM_002471.4(MYH6):c.1410C>T (p.Asp470=)	rs139886074	0.00011
NM_002471.4(MYH6):c.2973C>T (p.Ile991=)	rs374807345	0.00011
NM_002471.4(MYH6):c.678C>T (p.Pro226=)	rs768893926	0.00011
NM_002471.4(MYH6):c.1662C>T (p.Tyr554=)	rs374114140	0.00010
NM_002471.4(MYH6):c.3988G>A (p.Ala1330Thr)	rs757840030	0.00007
NM_002471.4(MYH6):c.1087A>T (p.Met363Leu)	rs202196487	0.00005
NM_002471.4(MYH6):c.5427A>C (p.Gly1809=)	rs149294569	0.00005
NM_002471.4(MYH6):c.5661+9A>G	rs373908250	0.00005
NM_002471.4(MYH6):c.1381C>T (p.Leu461=)	rs368609214	0.00004
NM_002471.4(MYH6):c.2127G>A (p.Lys709=)	rs765316931	0.00003
NM_002471.4(MYH6):c.1086C>T (p.Asn362=)	rs375189593	0.00002
NM_002471.4(MYH6):c.1575C>T (p.Ile525=)	rs756615422	0.00002
NM_002471.4(MYH6):c.2271G>A (p.Gln757=)	rs777100730	0.00002
NM_002471.4(MYH6):c.4470C>T (p.Tyr1490=)	rs727504964	0.00002
NM_002471.4(MYH6):c.1227C>T (p.Asn409=)	rs752919716	0.00001
NM_002471.4(MYH6):c.5623C>T (p.Leu1875=)	rs368604132	0.00001
NM_002471.3(MYH6):c.3979-8C>A	rs555976716
NM_002471.4(MYH6):c.1581+10del	rs560271582
NM_002471.4(MYH6):c.2736A>G (p.Lys912=)
NM_002471.4(MYH6):c.3979-10C>G	rs28730768
NM_002471.4(MYH6):c.3979-14C>A	rs372226248
NM_002471.4(MYH6):c.3979-3dup	rs770492637
NM_002471.4(MYH6):c.3979-7_3979-6del	rs796313537
NM_002471.4(MYH6):c.4595G>T (p.Arg1532Leu)	rs34330111

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