ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.4644+113G>A rs7146601 0.01490
NM_000257.4(MYH7):c.4645-220C>T rs7140743 0.01448
NM_000257.4(MYH7):c.4520-25C>T rs45503601 0.00787
NM_000257.4(MYH7):c.4645-273T>C rs146641667 0.00561
NM_000257.4(MYH7):c.4354-61A>T rs559916092 0.00559
NM_000257.4(MYH7):c.4520-79G>A rs147064810 0.00305
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101 0.00024
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934 0.00014
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242 0.00008
NM_000257.4(MYH7):c.4347C>T (p.Phe1449=) rs182311329 0.00005
NM_000257.4(MYH7):c.4353+23A>G rs533030007 0.00004
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720 0.00004
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=) rs781203524 0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664 0.00002
NM_000257.4(MYH7):c.4353+6C>T rs765398896 0.00001
NM_000257.4(MYH7):c.4371G>A (p.Lys1457=) rs1555336697 0.00001
NM_000257.4(MYH7):c.4520-3C>T rs549509054 0.00001
NM_000257.4(MYH7):c.4644+3G>A rs397516226 0.00001
NM_000257.4(MYH7):c.4644+7G>C rs1555336564 0.00001
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4275C>T (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213

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