ClinVar Miner

List of variants in gene MYH6 reported as likely benign by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
Download table as spreadsheet
HGVS dbSNP
NM_002471.3(MYH6):c.1935C>T (p.Ser645=) rs142393002
NM_002471.3(MYH6):c.2430-4C>A rs376527296
NM_002471.3(MYH6):c.3682C>T (p.Leu1228=) rs1033363939
NM_002471.3(MYH6):c.3867G>T (p.Leu1289Phe) rs138127105
NM_002471.3(MYH6):c.3979-9C>A rs57660219
NM_002471.3(MYH6):c.4359+10G>A rs368183862
NM_002471.3(MYH6):c.4665C>T (p.His1555=) rs373888186
NM_002471.4(MYH6):c.1131C>G (p.Asp377Glu) rs61742472
NM_002471.4(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser) rs148962966
NM_002471.4(MYH6):c.1200G>A (p.Leu400=)
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031
NM_002471.4(MYH6):c.2805C>T (p.Asn935=) rs757958461
NM_002471.4(MYH6):c.2806G>T (p.Ala936Ser) rs141704264
NM_002471.4(MYH6):c.2928+5G>A rs28730772
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.4(MYH6):c.3178G>A (p.Asp1060Asn)
NM_002471.4(MYH6):c.3447C>G (p.Ser1149Arg) rs564367705
NM_002471.4(MYH6):c.3627C>T (p.Ile1209=) rs147871745
NM_002471.4(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.4(MYH6):c.3927T>C (p.Ser1309=) rs115742584
NM_002471.4(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.4(MYH6):c.4320T>A (p.Ala1440=) rs145566711
NM_002471.4(MYH6):c.4611G>A (p.Val1537=) rs142983918
NM_002471.4(MYH6):c.4782G>A (p.Arg1594=) rs142823394
NM_002471.4(MYH6):c.4960-9G>A rs557113705
NM_002471.4(MYH6):c.5514G>T (p.Ser1838=) rs727503232
NM_002471.4(MYH6):c.643-5C>T rs199859986
NM_002471.4(MYH6):c.693C>T (p.Phe231=)

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.