ClinVar Miner

List of variants in gene combination LOC126861896, MYH6 reported as likely benign for hypertrophic cardiomyopathy

Included ClinVar conditions (244):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.4906C>T (p.Arg1636Cys) rs149460065 0.00116
NM_002471.4(MYH6):c.4905C>T (p.Asn1635=) rs143048583 0.00043
NM_002471.4(MYH6):c.5140C>A (p.Arg1714=) rs140651265 0.00036
NM_002471.4(MYH6):c.5112G>A (p.Ala1704=) rs150450178 0.00031
NM_002471.4(MYH6):c.4812T>C (p.Asp1604=) rs201667127 0.00016
NM_002471.4(MYH6):c.4833C>T (p.Asn1611=) rs139329956 0.00009
NM_002471.4(MYH6):c.4651-4C>A rs766134513 0.00008
NM_002471.4(MYH6):c.5085G>A (p.Glu1695=) rs1206016022 0.00008
NM_002471.4(MYH6):c.4651-14C>A rs902807471 0.00006
NM_002471.4(MYH6):c.5077G>A (p.Val1693Met) rs373457153 0.00005
NM_002471.4(MYH6):c.4695A>G (p.Leu1565=) rs374702183 0.00004
NM_002471.4(MYH6):c.4722C>T (p.Ile1574=) rs375410722 0.00004
NM_002471.4(MYH6):c.4791C>T (p.Asp1597=) rs761627508 0.00004
NM_002471.4(MYH6):c.5001C>T (p.Asp1667=) rs377698958 0.00004
NM_002471.4(MYH6):c.5067G>A (p.Glu1689=) rs202210008 0.00004
NM_002471.4(MYH6):c.4959+12C>T rs371661383 0.00003
NM_002471.4(MYH6):c.4983T>C (p.Asp1661=) rs763573894 0.00003
NM_002471.4(MYH6):c.4842G>A (p.Leu1614=) rs763639676 0.00002
NM_002471.4(MYH6):c.5076C>T (p.Ala1692=) rs377569988 0.00002
NM_002471.4(MYH6):c.5136C>T (p.Ser1712=) rs397516774 0.00002
NM_002471.4(MYH6):c.4651-9C>A rs1427589559 0.00001
NM_002471.4(MYH6):c.4698G>A (p.Glu1566=) rs542799440 0.00001
NM_002471.4(MYH6):c.4839C>T (p.Val1613=) rs753478528 0.00001
NM_002471.4(MYH6):c.4923C>T (p.Ala1641=) rs755556624 0.00001
NM_002471.4(MYH6):c.4959+20C>G rs1891018867 0.00001
NM_002471.4(MYH6):c.4971C>T (p.Ile1657=) rs566793615 0.00001
NM_002471.4(MYH6):c.5020G>A (p.Ala1674Thr) rs534560839 0.00001
NM_002471.4(MYH6):c.5025C>T (p.Ile1675=) rs763337280 0.00001
NM_002471.4(MYH6):c.5142G>A (p.Arg1714=) rs755986916 0.00001
NM_002471.4(MYH6):c.4653C>T (p.Ala1551=) rs2138585541
NM_002471.4(MYH6):c.4665C>T (p.His1555=) rs373888186
NM_002471.4(MYH6):c.4674C>T (p.Gly1558=)
NM_002471.4(MYH6):c.4728G>A (p.Arg1576=)
NM_002471.4(MYH6):c.4788G>A (p.Val1596=)
NM_002471.4(MYH6):c.4794G>A (p.Ser1598=)
NM_002471.4(MYH6):c.4854G>A (p.Lys1618=) rs766153681
NM_002471.4(MYH6):c.4866A>G (p.Gly1622=)
NM_002471.4(MYH6):c.4926G>A (p.Gln1642=)
NM_002471.4(MYH6):c.4959+11G>A
NM_002471.4(MYH6):c.4959+13G>T rs28730765
NM_002471.4(MYH6):c.4959+15G>A
NM_002471.4(MYH6):c.4959+20C>T
NM_002471.4(MYH6):c.4977G>A (p.Leu1659=)
NM_002471.4(MYH6):c.4995C>T (p.Ala1665=) rs746503024
NM_002471.4(MYH6):c.5019C>A (p.Ile1673=)
NM_002471.4(MYH6):c.5068C>T (p.Leu1690=)
NM_002471.4(MYH6):c.5133C>G (p.Thr1711=) rs775234352
NM_002471.4(MYH6):c.5148G>A (p.Gln1716=) rs936703258
NM_002471.4(MYH6):c.5163+15A>G

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