ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 131
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101 0.00024
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys) rs139646545 0.00009
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242 0.00008
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244 0.00006
NM_000257.4(MYH7):c.4353+5G>A rs200436876 0.00006
NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373 0.00006
NM_000257.4(MYH7):c.4294G>A (p.Val1432Ile) rs144200285 0.00005
NM_000257.4(MYH7):c.4519+6C>T rs370779504 0.00005
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211 0.00004
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720 0.00004
NM_000257.4(MYH7):c.4499G>A (p.Arg1500Gln) rs121913647 0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664 0.00002
NM_000257.4(MYH7):c.4558G>A (p.Gly1520Arg) rs763683589 0.00002
NM_000257.4(MYH7):c.4301G>A (p.Arg1434His) rs780625785 0.00001
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245 0.00001
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341 0.00001
NM_000257.4(MYH7):c.4353+6C>T rs765398896 0.00001
NM_000257.4(MYH7):c.4354-5G>A rs950409210 0.00001
NM_000257.4(MYH7):c.4364A>G (p.Glu1455Gly) rs771377530 0.00001
NM_000257.4(MYH7):c.4373A>G (p.Gln1458Arg) rs772562745 0.00001
NM_000257.4(MYH7):c.4388C>T (p.Ser1463Leu) rs890401818 0.00001
NM_000257.4(MYH7):c.4390C>T (p.Gln1464Ter) rs754829218 0.00001
NM_000257.4(MYH7):c.4394C>T (p.Ser1465Leu) rs1033511138 0.00001
NM_000257.4(MYH7):c.4435A>G (p.Thr1479Ala) rs752867429 0.00001
NM_000257.4(MYH7):c.4440G>T (p.Glu1480Asp) rs1351661186 0.00001
NM_000257.4(MYH7):c.4450C>A (p.Leu1484Ile) rs1555336651 0.00001
NM_000257.4(MYH7):c.4459G>A (p.Ala1487Thr) rs766909770 0.00001
NM_000257.4(MYH7):c.4481A>T (p.His1494Leu) rs727505329 0.00001
NM_000257.4(MYH7):c.4489A>T (p.Thr1497Ser) rs928227757 0.00001
NM_000257.4(MYH7):c.4519+1G>C rs876661374 0.00001
NM_000257.4(MYH7):c.4520-3C>T rs549509054 0.00001
NM_000257.4(MYH7):c.4525A>C (p.Ile1509Leu) rs397516221 0.00001
NM_000257.4(MYH7):c.4531G>A (p.Asp1511Asn) rs1219074705 0.00001
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225 0.00001
NM_000257.4(MYH7):c.4606G>A (p.Glu1536Lys) rs779315151 0.00001
NM_000257.4(MYH7):c.4264C>A (p.Gln1422Lys)
NM_000257.4(MYH7):c.4270G>A (p.Glu1424Lys) rs730880798
NM_000257.4(MYH7):c.4271A>T (p.Glu1424Val)
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys) rs397516208
NM_000257.4(MYH7):c.4279G>T (p.Asp1427Tyr)
NM_000257.4(MYH7):c.4285_4287del (p.Met1429del) rs1892274161
NM_000257.4(MYH7):c.4286T>C (p.Met1429Thr)
NM_000257.4(MYH7):c.4286TGG[1] (p.Val1430del) rs1555336747
NM_000257.4(MYH7):c.4292A>G (p.Asp1431Gly) rs776921449
NM_000257.4(MYH7):c.4300C>T (p.Arg1434Cys) rs730880800
NM_000257.4(MYH7):c.4301G>T (p.Arg1434Leu)
NM_000257.4(MYH7):c.4306A>G (p.Asn1436Asp) rs1892272742
NM_000257.4(MYH7):c.4307A>G (p.Asn1436Ser) rs1489767429
NM_000257.4(MYH7):c.4308TGC[5] (p.Ala1441dup) rs1892272029
NM_000257.4(MYH7):c.4312G>C (p.Ala1438Pro)
NM_000257.4(MYH7):c.4325T>C (p.Leu1442Pro) rs2138646429
NM_000257.4(MYH7):c.4327G>C (p.Asp1443His) rs2138646412
NM_000257.4(MYH7):c.4330AAG[1] (p.Lys1445del)
NM_000257.4(MYH7):c.4343A>G (p.Asn1448Ser) rs753484341
NM_000257.4(MYH7):c.4347C>G (p.Phe1449Leu) rs182311329
NM_000257.4(MYH7):c.4352A>C (p.Lys1451Thr)
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4357C>G (p.Leu1453Val)
NM_000257.4(MYH7):c.4360G>A (p.Ala1454Thr) rs1358268382
NM_000257.4(MYH7):c.4361C>A (p.Ala1454Asp) rs1892259980
NM_000257.4(MYH7):c.4371G>C (p.Lys1457Asn) rs1555336697
NM_000257.4(MYH7):c.4372C>G (p.Gln1458Glu)
NM_000257.4(MYH7):c.4379A>G (p.Tyr1460Cys)
NM_000257.4(MYH7):c.4381G>A (p.Glu1461Lys) rs2138645640
NM_000257.4(MYH7):c.4382A>G (p.Glu1461Gly) rs995126992
NM_000257.4(MYH7):c.4384G>A (p.Glu1462Lys) rs1892258263
NM_000257.4(MYH7):c.4395G>A (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4396G>T (p.Glu1466Ter)
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4409C>T (p.Ser1470Leu) rs1468116782
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4414_4416del (p.Lys1472del) rs1555336672
NM_000257.4(MYH7):c.4420G>C (p.Ala1474Pro)
NM_000257.4(MYH7):c.4424G>C (p.Arg1475Pro)
NM_000257.4(MYH7):c.4427C>T (p.Ser1476Phe) rs1566525169
NM_000257.4(MYH7):c.4429C>A (p.Leu1477Ile) rs1892255625
NM_000257.4(MYH7):c.4436C>T (p.Thr1479Ile) rs397516217
NM_000257.4(MYH7):c.4451T>C (p.Leu1484Pro) rs1595074765
NM_000257.4(MYH7):c.4453A>C (p.Lys1485Gln)
NM_000257.4(MYH7):c.4454A>G (p.Lys1485Arg) rs1566525134
NM_000257.4(MYH7):c.4458C>A (p.Asn1486Lys) rs571704020
NM_000257.4(MYH7):c.4459G>T (p.Ala1487Ser) rs766909770
NM_000257.4(MYH7):c.4460C>T (p.Ala1487Val) rs1595074732
NM_000257.4(MYH7):c.4461C>G (p.Ala1487=) rs2138645345
NM_000257.4(MYH7):c.4463A>G (p.Tyr1488Cys) rs948329167
NM_000257.4(MYH7):c.4465G>A (p.Glu1489Lys)
NM_000257.4(MYH7):c.4465GAG[3] (p.Glu1490dup) rs1566525106
NM_000257.4(MYH7):c.4466A>G (p.Glu1489Gly)
NM_000257.4(MYH7):c.4467G>C (p.Glu1489Asp) rs1892253421
NM_000257.4(MYH7):c.4475T>C (p.Leu1492Pro) rs1892252730
NM_000257.4(MYH7):c.4477G>T (p.Glu1493Ter) rs2138645254
NM_000257.4(MYH7):c.4483C>G (p.Leu1495Val) rs1892252122
NM_000257.4(MYH7):c.4484T>C (p.Leu1495Pro) rs1566525081
NM_000257.4(MYH7):c.4493_4494delinsAT (p.Phe1498Tyr) rs2138645175
NM_000257.4(MYH7):c.4501G>T (p.Glu1501Ter) rs1595074652
NM_000257.4(MYH7):c.4506del (p.Asn1502fs) rs2138645134
NM_000257.4(MYH7):c.4510A>T (p.Asn1504Tyr) rs869025482
NM_000257.4(MYH7):c.4511A>C (p.Asn1504Thr) rs1892250074
NM_000257.4(MYH7):c.4519+3G>T rs1566525012
NM_000257.4(MYH7):c.4520-1G>T rs730880801
NM_000257.4(MYH7):c.4521G>C (p.Glu1507Asp)
NM_000257.4(MYH7):c.4524G>C (p.Glu1508Asp) rs1033543834
NM_000257.4(MYH7):c.4526T>A (p.Ile1509Asn) rs2138644579
NM_000257.4(MYH7):c.4527C>G (p.Ile1509Met) rs781223723
NM_000257.4(MYH7):c.4532A>T (p.Asp1511Val) rs730880802
NM_000257.4(MYH7):c.4537A>T (p.Thr1513Ser) rs397516222
NM_000257.4(MYH7):c.4541A>G (p.Glu1514Gly) rs1351712658
NM_000257.4(MYH7):c.4543C>A (p.Gln1515Lys)
NM_000257.4(MYH7):c.4543C>G (p.Gln1515Glu) rs1892239000
NM_000257.4(MYH7):c.4553C>A (p.Ser1518Tyr) rs757809347
NM_000257.4(MYH7):c.4562A>G (p.Lys1521Arg) rs1892238144
NM_000257.4(MYH7):c.4564A>G (p.Thr1522Ala)
NM_000257.4(MYH7):c.4565C>T (p.Thr1522Ile) rs2138644446
NM_000257.4(MYH7):c.4567A>G (p.Ile1523Val) rs1555336580
NM_000257.4(MYH7):c.4568T>C (p.Ile1523Thr) rs1892237828
NM_000257.4(MYH7):c.4571A>C (p.His1524Pro) rs767148171
NM_000257.4(MYH7):c.4571A>G (p.His1524Arg) rs767148171
NM_000257.4(MYH7):c.4584_4585delinsAT (p.Val1529Phe) rs1892237017
NM_000257.4(MYH7):c.4589G>A (p.Arg1530Gln) rs730880803
NM_000257.4(MYH7):c.4611G>T (p.Lys1537Asn) rs1892235698
NM_000257.4(MYH7):c.4622A>C (p.Gln1541Pro) rs587779389
NM_000257.4(MYH7):c.4622A>T (p.Gln1541Leu) rs587779389
NM_000257.4(MYH7):c.4628C>T (p.Ala1543Val) rs1892235051
NM_000257.4(MYH7):c.4630C>A (p.Leu1544Met) rs1595074238
NM_000257.4(MYH7):c.4631T>C (p.Leu1544Pro) rs1892234748
NM_000257.4(MYH7):c.4639G>A (p.Ala1547Thr) rs2138644219
NM_000257.4(MYH7):c.4643A>C (p.Glu1548Ala) rs730880804
NM_000257.4(MYH7):c.4643A>T (p.Glu1548Val) rs730880804
NM_000257.4(MYH7):c.4644+11_4644+12delinsAG
NM_000257.4(MYH7):c.4644+5G>C rs730880797
NM_000257.4(MYH7):c.4644+5G>T

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