ClinVar Miner

List of variants reported as benign for hypertrophic cardiomyopathy 14

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 114
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.800-11A>G rs434273 0.81807
NM_002471.4(MYH6):c.4914T>C (p.Ala1638=) rs178640 0.53346
NM_002471.4(MYH6):c.4359+13C>T rs8022522 0.46131
NM_002471.4(MYH6):c.3302T>C (p.Val1101Ala) rs365990 0.44987
NM_002471.4(MYH6):c.2292+18C>T rs452036 0.42619
NM_002471.4(MYH6):c.4651-17G>A rs2071634 0.23331
NM_002471.4(MYH6):c.411G>A (p.Glu137=) rs2277474 0.22054
NM_002471.4(MYH6):c.3388G>A (p.Ala1130Thr) rs28730771 0.08821
NM_002471.4(MYH6):c.5598A>G (p.Leu1866=) rs17091278 0.08756
NM_002471.4(MYH6):c.4011G>A (p.Ser1337=) rs451794 0.07834
NM_002471.4(MYH6):c.4980C>T (p.Asp1660=) rs382872 0.07807
NM_002471.4(MYH6):c.5259C>T (p.Ala1753=) rs8004990 0.07782
NM_002471.4(MYH6):c.393G>A (p.Leu131=) rs17277970 0.06973
NM_002471.4(MYH6):c.166G>A (p.Gly56Arg) rs28711516 0.06950
NM_002471.4(MYH6):c.201+16C>T rs7147244 0.06154
NM_002471.4(MYH6):c.1335C>T (p.Asn445=) rs61731179 0.03984
NM_002471.4(MYH6):c.4960-17A>T rs28730764 0.03950
NM_002471.4(MYH6):c.4838T>C (p.Val1613Ala) rs61742476 0.03922
NM_002471.4(MYH6):c.4778A>T (p.Gln1593Leu) rs45574136 0.03900
NM_002471.4(MYH6):c.999C>T (p.Thr333=) rs78107039 0.03596
NM_002471.4(MYH6):c.909G>A (p.Leu303=) rs17091623 0.02711
NM_002471.4(MYH6):c.4527G>A (p.Glu1509=) rs34855944 0.02632
NM_002471.4(MYH6):c.3408G>A (p.Lys1136=) rs28730770 0.01687
NM_002471.4(MYH6):c.2151C>T (p.Tyr717=) rs76202964 0.01414
NM_002471.4(MYH6):c.3979-7del rs397516766 0.01401
NM_002471.4(MYH6):c.399G>A (p.Val133=) rs78891557 0.01343
NM_002471.4(MYH6):c.2946G>A (p.Glu982=) rs145274612 0.01048
NM_002471.4(MYH6):c.3627C>T (p.Ile1209=) rs147871745 0.00930
NM_002471.4(MYH6):c.3480C>T (p.Ser1160=) rs373345984 0.00929
NM_002471.4(MYH6):c.4959+13G>A rs28730765 0.00762
NM_002471.4(MYH6):c.4206C>T (p.Ala1402=) rs111638554 0.00728
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031 0.00573
NM_002471.4(MYH6):c.4899C>T (p.His1633=) rs61742474 0.00517
NM_002471.4(MYH6):c.330G>A (p.Ala110=) rs77679218 0.00490
NM_002471.4(MYH6):c.36G>A (p.Ala12=) rs141014719 0.00487
NM_002471.4(MYH6):c.86G>A (p.Arg29Gln) rs150574114 0.00455
NM_002471.4(MYH6):c.1989C>T (p.Asn663=) rs28730774 0.00451
NM_002471.4(MYH6):c.2168+17C>A rs192337153 0.00443
NM_002471.4(MYH6):c.622G>A (p.Asp208Asn) rs142027794 0.00415
NM_002471.4(MYH6):c.4651-12A>C rs193922653 0.00413
NM_002471.4(MYH6):c.4395G>A (p.Ser1465=) rs74039310 0.00368
NM_002471.4(MYH6):c.5475G>A (p.Glu1825=) rs79143968 0.00344
NM_002471.4(MYH6):c.1071C>T (p.Ile357=) rs58131640 0.00309
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile) rs148915045 0.00284
NM_002471.4(MYH6):c.1449C>T (p.Asn483=) rs145447555 0.00238
NM_002471.4(MYH6):c.1275C>T (p.Ile425=) rs61742470 0.00232
NM_002471.4(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550 0.00217
NM_002471.4(MYH6):c.3979-7dup rs545343612 0.00208
NM_002471.4(MYH6):c.4416A>G (p.Ser1472=) rs140800076 0.00199
NM_002471.4(MYH6):c.4320T>A (p.Ala1440=) rs145566711 0.00189
NM_002471.4(MYH6):c.2293-12C>G rs115453571 0.00175
NM_002471.4(MYH6):c.2928+5G>A rs28730772 0.00172
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala) rs142992009 0.00153
NM_002471.4(MYH6):c.2890G>T (p.Ala964Ser) rs144907522 0.00148
NM_002471.4(MYH6):c.3979-15C>A rs529249069 0.00146
NM_002471.4(MYH6):c.3927T>C (p.Ser1309=) rs115742584 0.00145
NM_002471.4(MYH6):c.5400C>T (p.Asp1800=) rs144329079 0.00141
NM_002471.4(MYH6):c.4782G>A (p.Arg1594=) rs142823394 0.00130
NM_002471.4(MYH6):c.1122G>A (p.Ala374=) rs148091079 0.00116
NM_002471.4(MYH6):c.2430-14C>T rs190342289 0.00108
NM_002471.4(MYH6):c.1083G>T (p.Gly361=) rs138928022 0.00092
NM_002471.4(MYH6):c.3297G>A (p.Glu1099=) rs144957142 0.00090
NM_002471.4(MYH6):c.3978+8C>T rs367866050 0.00088
NM_002471.4(MYH6):c.735+16C>T rs76202841 0.00080
NM_002471.4(MYH6):c.2807C>T (p.Ala936Val) rs199838024 0.00067
NM_002471.4(MYH6):c.4986G>A (p.Ala1662=) rs77416370 0.00066
NM_002471.4(MYH6):c.1779C>A (p.Gly593=) rs190996339 0.00065
NM_002471.4(MYH6):c.5601G>A (p.Gln1867=) rs148984154 0.00062
NM_002471.4(MYH6):c.5652C>T (p.Ala1884=) rs200662317 0.00062
NM_002471.4(MYH6):c.3573C>T (p.Ala1191=) rs727505358 0.00054
NM_002471.4(MYH6):c.1141+8G>T rs377327277 0.00045
NM_002471.4(MYH6):c.210T>C (p.Thr70=) rs147397431 0.00041
NM_002471.4(MYH6):c.492C>T (p.Tyr164=) rs201380776 0.00041
NM_002471.4(MYH6):c.4136C>T (p.Thr1379Met) rs145611185 0.00036
NM_002471.4(MYH6):c.5140C>A (p.Arg1714=) rs140651265 0.00036
NM_002471.4(MYH6):c.4359+5A>G rs193283041 0.00031
NM_002471.4(MYH6):c.4293G>A (p.Met1431Ile) rs201016285 0.00029
NM_002471.4(MYH6):c.642+16C>T rs547762012 0.00025
NM_002471.4(MYH6):c.4536G>A (p.Ser1512=) rs142539180 0.00018
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser) rs148962966 0.00014
NM_002471.4(MYH6):c.2429+14A>C rs200817451 0.00014
NM_002471.4(MYH6):c.3979-13C>A rs563648655 0.00013
NM_002471.4(MYH6):c.939C>T (p.Phe313=) rs372589578 0.00007
NM_002471.4(MYH6):c.3932C>T (p.Thr1311Ile) rs535425638 0.00006
NM_002471.4(MYH6):c.4245A>G (p.Ser1415=) rs779697115 0.00006
NM_002471.4(MYH6):c.3508G>A (p.Glu1170Lys) rs727503236 0.00003
NM_002471.4(MYH6):c.5439G>A (p.Gln1813=) rs200854143 0.00002
NM_002471.4(MYH6):c.4960-9G>A rs557113705 0.00001
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.2806G>T (p.Ala936Ser) rs141704264
NM_002471.4(MYH6):c.3302_3303inv (p.Val1101Ala)
NM_002471.4(MYH6):c.3342+12del
NM_002471.4(MYH6):c.3343-20G>A
NM_002471.4(MYH6):c.3609C>G (p.Ala1203=) rs149369904
NM_002471.4(MYH6):c.3979-11C>G rs200618133
NM_002471.4(MYH6):c.3979-17_3979-16dup rs193922652
NM_002471.4(MYH6):c.3979-3dup rs770492637
NM_002471.4(MYH6):c.3979-7T>C rs535111647
NM_002471.4(MYH6):c.3979-8C>G rs555976716
NM_002471.4(MYH6):c.3979-8C>T rs555976716
NM_002471.4(MYH6):c.3979-8del rs193922652
NM_002471.4(MYH6):c.3979-8dup rs193922652
NM_002471.4(MYH6):c.3979-9C>A rs57660219
NM_002471.4(MYH6):c.3979-9C>G rs57660219
NM_002471.4(MYH6):c.3979-9_3979-8del rs193922652
NM_002471.4(MYH6):c.427C>A (p.Arg143=) rs2277473
NM_002471.4(MYH6):c.4360-7C>G rs58949384
NM_002471.4(MYH6):c.4360-7C>T rs58949384
NM_002471.4(MYH6):c.4683C>T (p.Leu1561=) rs559319718
NM_002471.4(MYH6):c.4959+11del rs753018745
NM_002471.4(MYH6):c.502+14C>A
NM_002471.4(MYH6):c.503-10_503-8del
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile) rs573489857

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