ClinVar Miner

List of variants in gene MYH6 studied for Hypertrophic cardiomyopathy

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Total variants: 106
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HGVS dbSNP
NM_002471.3(MYH6):c.1007C>G (p.Ala336Gly) rs138572790
NM_002471.3(MYH6):c.1071C>T (p.Ile357=) rs58131640
NM_002471.3(MYH6):c.1122G>A (p.Ala374=) rs148091079
NM_002471.3(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.3(MYH6):c.1244G>C (p.Gly415Ala) rs759520932
NM_002471.3(MYH6):c.1335C>T (p.Asn445=) rs61731179
NM_002471.3(MYH6):c.1410C>T (p.Asp470=) rs139886074
NM_002471.3(MYH6):c.1520T>G (p.Ile507Ser) rs188023690
NM_002471.3(MYH6):c.1551C>A (p.Asp517Glu)
NM_002471.3(MYH6):c.1588G>A (p.Gly530Ser) rs886050411
NM_002471.3(MYH6):c.1716G>A (p.Gly572=) rs886050410
NM_002471.3(MYH6):c.1753G>A (p.Gly585Ser) rs150415679
NM_002471.3(MYH6):c.1809C>T (p.Asn603=) rs186134696
NM_002471.3(MYH6):c.1822G>A (p.Ala608Thr) rs886050409
NM_002471.3(MYH6):c.1944G>A (p.Thr648=) rs367742240
NM_002471.3(MYH6):c.2097C>T (p.Gly699=) rs149734381
NM_002471.3(MYH6):c.2141G>A (p.Arg714His) rs776602843
NM_002471.3(MYH6):c.2151C>T (p.Tyr717=) rs76202964
NM_002471.3(MYH6):c.2363C>T (p.Thr788Met) rs746758304
NM_002471.3(MYH6):c.2398C>T (p.Arg800Cys) rs763477425
NM_002471.3(MYH6):c.2430-14C>T rs190342289
NM_002471.3(MYH6):c.2440C>A (p.Leu814Met) rs150675144
NM_002471.3(MYH6):c.2540C>T (p.Thr847Met) rs759408374
NM_002471.3(MYH6):c.2685+14A>T rs765118655
NM_002471.3(MYH6):c.2685+15T>C rs368883537
NM_002471.3(MYH6):c.2806G>T (p.Ala936Ser) rs141704264
NM_002471.3(MYH6):c.2827C>T (p.Arg943Cys) rs368912844
NM_002471.3(MYH6):c.2928+5G>A rs28730772
NM_002471.3(MYH6):c.2946G>A (p.Glu982=) rs145274612
NM_002471.3(MYH6):c.3164G>A (p.Arg1055Gln) rs540893860
NM_002471.3(MYH6):c.3195G>C (p.Gln1065His) rs267606904
NM_002471.3(MYH6):c.3199A>G (p.Ser1067Gly) rs145508517
NM_002471.3(MYH6):c.3220G>A (p.Asp1074Asn) rs375169402
NM_002471.3(MYH6):c.3302T>C (p.Val1101Ala) rs365990
NM_002471.3(MYH6):c.3388G>A (p.Ala1130Thr) rs28730771
NM_002471.3(MYH6):c.3408G>A (p.Lys1136=) rs28730770
NM_002471.3(MYH6):c.3421C>T (p.Leu1141=) rs757043117
NM_002471.3(MYH6):c.3428G>A (p.Arg1143Gln) rs543585784
NM_002471.3(MYH6):c.3476C>T (p.Thr1159Met) rs780305056
NM_002471.3(MYH6):c.3480C>T (p.Ser1160=) rs373345984
NM_002471.3(MYH6):c.3481G>A (p.Val1161Met) rs762230455
NM_002471.3(MYH6):c.3500A>C (p.Lys1167Thr) rs775248044
NM_002471.3(MYH6):c.3569C>T (p.Thr1190Ile) rs759117852
NM_002471.3(MYH6):c.3583C>T (p.Arg1195Cys) rs769756450
NM_002471.3(MYH6):c.3604G>A (p.Val1202Met) rs368451573
NM_002471.3(MYH6):c.3609C>G (p.Ala1203=) rs149369904
NM_002471.3(MYH6):c.3627C>T (p.Ile1209=) rs147871745
NM_002471.3(MYH6):c.3978+8C>T rs367866050
NM_002471.3(MYH6):c.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-10C>G rs28730768
NM_002471.3(MYH6):c.3979-11C>G rs200618133
NM_002471.3(MYH6):c.3979-12C>A rs754263361
NM_002471.3(MYH6):c.3979-14C>A rs372226248
NM_002471.3(MYH6):c.3979-17dup rs193922652
NM_002471.3(MYH6):c.3979-7delT rs397516766
NM_002471.3(MYH6):c.3979-8C>A rs555976716
NM_002471.3(MYH6):c.3979-8C>T rs555976716
NM_002471.3(MYH6):c.3979-8delC rs193922652
NM_002471.3(MYH6):c.4011G>A (p.Ser1337=) rs451794
NM_002471.3(MYH6):c.4062G>A (p.Glu1354=) rs754664098
NM_002471.3(MYH6):c.4167A>G (p.Glu1389=) rs763070661
NM_002471.3(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.3(MYH6):c.4206C>T (p.Ala1402=) rs111638554
NM_002471.3(MYH6):c.4293G>A (p.Met1431Ile) rs201016285
NM_002471.3(MYH6):c.4320T>A (p.Ala1440=) rs145566711
NM_002471.3(MYH6):c.4328C>A (p.Ala1443Asp) rs727503234
NM_002471.3(MYH6):c.4359+10G>A rs368183862
NM_002471.3(MYH6):c.4359+13C>T rs8022522
NM_002471.3(MYH6):c.4360-7C>T rs58949384
NM_002471.3(MYH6):c.4527G>A (p.Glu1509=) rs34855944
NM_002471.3(MYH6):c.4651-12A>C rs193922653
NM_002471.3(MYH6):c.4695A>G (p.Leu1565=) rs374702183
NM_002471.3(MYH6):c.4778A>T (p.Gln1593Leu) rs45574136
NM_002471.3(MYH6):c.4780C>T (p.Arg1594Trp)
NM_002471.3(MYH6):c.4829G>A (p.Arg1610His) rs758792342
NM_002471.3(MYH6):c.4838T>C (p.Val1613Ala) rs61742476
NM_002471.3(MYH6):c.4906C>T (p.Arg1636Cys) rs149460065
NM_002471.3(MYH6):c.4914T>C (p.Ala1638=) rs178640
NM_002471.3(MYH6):c.4959+12C>T rs371661383
NM_002471.3(MYH6):c.4959+13G>A rs28730765
NM_002471.3(MYH6):c.4960-9G>A rs557113705
NM_002471.3(MYH6):c.4980C>T (p.Asp1660=) rs382872
NM_002471.3(MYH6):c.4999G>A (p.Asp1667Asn) rs758251388
NM_002471.3(MYH6):c.5072G>A (p.Arg1691His) rs727504502
NM_002471.3(MYH6):c.5112G>A (p.Ala1704=) rs150450178
NM_002471.3(MYH6):c.5259C>T (p.Ala1753=) rs8004990
NM_002471.3(MYH6):c.5260G>C (p.Glu1754Gln) rs372270600
NM_002471.3(MYH6):c.5347C>T (p.Arg1783Cys) rs758734120
NM_002471.3(MYH6):c.5367G>A (p.Glu1789=) rs753335327
NM_002471.3(MYH6):c.5403G>A (p.Glu1801=) rs762151922
NM_002471.3(MYH6):c.5410C>A (p.Gln1804Lys) rs144571463
NM_002471.3(MYH6):c.5439G>A (p.Gln1813=) rs200854143
NM_002471.3(MYH6):c.5475G>A (p.Glu1825=) rs79143968
NM_002471.3(MYH6):c.5500C>T (p.Arg1834Cys) rs137923514
NM_002471.3(MYH6):c.5566-7C>T rs200509899
NM_002471.3(MYH6):c.5587C>T (p.Leu1863=) rs142767538
NM_002471.3(MYH6):c.5598A>G (p.Leu1866=) rs17091278
NM_002471.3(MYH6):c.5652C>T (p.Ala1884=) rs200662317
NM_002471.3(MYH6):c.675C>T (p.Asn225=) rs886050413
NM_002471.3(MYH6):c.800-11A>G rs434273
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.3(MYH6):c.899-15C>T rs886050412
NM_002471.3(MYH6):c.909G>A (p.Leu303=) rs17091623
NM_002471.3(MYH6):c.934G>A (p.Ala312Thr) rs748143404
NM_002471.3(MYH6):c.981C>T (p.Ser327=) rs148407931
NM_002471.3(MYH6):c.999C>T (p.Thr333=) rs78107039

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