ClinVar Miner

List of variants in gene MYH7 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781
NM_000257.4(MYH7):c.1062C>T (p.Gly354=) rs735712
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1230C>T (p.Tyr410=) rs150885220
NM_000257.4(MYH7):c.1407T>C (p.Asp469=) rs112172952
NM_000257.4(MYH7):c.1408-117C>T
NM_000257.4(MYH7):c.1482T>C (p.Phe494=) rs587781088
NM_000257.4(MYH7):c.153C>T (p.Ile51=) rs373145667
NM_000257.4(MYH7):c.1578+202A>G
NM_000257.4(MYH7):c.1578+243C>T
NM_000257.4(MYH7):c.1632C>T (p.Thr544=) rs587781089
NM_000257.4(MYH7):c.1767C>T (p.Asn589=) rs3729816
NM_000257.4(MYH7):c.189C>T (p.Thr63=) rs2069540
NM_000257.4(MYH7):c.201+121T>C
NM_000257.4(MYH7):c.2045-189G>T
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523
NM_000257.4(MYH7):c.2163-16A>T rs199538267
NM_000257.4(MYH7):c.2184G>A (p.Ala728=) rs148650290
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.2358G>A (p.Thr786=) rs36211714
NM_000257.4(MYH7):c.2358G>T (p.Thr786=) rs36211714
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.2553C>A (p.Ser851=) rs144291282
NM_000257.4(MYH7):c.261C>T (p.Ile87=) rs148560996
NM_000257.4(MYH7):c.2679+263T>G
NM_000257.4(MYH7):c.2679+7C>T rs368653983
NM_000257.4(MYH7):c.2680-95C>T
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2907C>T (p.His969=) rs142573531
NM_000257.4(MYH7):c.2922+82C>T
NM_000257.4(MYH7):c.2922G>A (p.Lys974=) rs147727900
NM_000257.4(MYH7):c.2923-6C>T rs587781082
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.2967T>C (p.Ile989=) rs7157716
NM_000257.4(MYH7):c.297C>T (p.Pro99=) rs140245862
NM_000257.4(MYH7):c.3099+175A>G
NM_000257.4(MYH7):c.3245+124T>C
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408
NM_000257.4(MYH7):c.3402G>A (p.Lys1134=) rs587781083
NM_000257.4(MYH7):c.3474C>T (p.Ser1158=) rs587780395
NM_000257.4(MYH7):c.3564T>C (p.Thr1188=) rs45587932
NM_000257.4(MYH7):c.3603C>G (p.Ala1201=) rs201576345
NM_000257.4(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.3864C>G (p.Ser1288=) rs45501694
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.3972+203G>A
NM_000257.4(MYH7):c.3973-249G>A
NM_000257.4(MYH7):c.3973-250C>T
NM_000257.4(MYH7):c.3993C>T (p.His1331=) rs200288088
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=) rs144465613
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.5283+19C>T rs45582836
NM_000257.4(MYH7):c.530+107C>A
NM_000257.4(MYH7):c.530+139A>G
NM_000257.4(MYH7):c.531-174C>T
NM_000257.4(MYH7):c.5361A>G (p.Glu1787=) rs201171029
NM_000257.4(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5559+67A>T
NM_000257.4(MYH7):c.5560-12T>G rs587781086
NM_000257.4(MYH7):c.5560-288C>T
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5574G>A (p.Arg1858=) rs529784690
NM_000257.4(MYH7):c.5646C>T (p.Ala1882=) rs730880726
NM_000257.4(MYH7):c.5661G>A (p.Glu1887=) rs730880727
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233
NM_000257.4(MYH7):c.5790+113T>C
NM_000257.4(MYH7):c.5790+15T>G rs199975761
NM_000257.4(MYH7):c.5791-106A>C
NM_000257.4(MYH7):c.5791-222G>A
NM_000257.4(MYH7):c.633G>A (p.Pro211=) rs587781087
NM_000257.4(MYH7):c.714C>T (p.Asn238=) rs202141819
NM_000257.4(MYH7):c.732C>T (p.Phe244=) rs2069542
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342

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