ClinVar Miner

List of variants in gene MYH7 reported as benign for Hypertrophic cardiomyopathy

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.189C>T (p.Thr63=) rs2069540 0.51584
NM_000257.4(MYH7):c.2967T>C (p.Ile989=) rs7157716 0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=) rs2069542 0.27385
NM_000257.4(MYH7):c.1128C>T (p.Asp376=) rs2231126 0.15761
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711 0.13859
NM_000257.4(MYH7):c.1062C>T (p.Gly354=) rs735712 0.06133
NM_000257.4(MYH7):c.2923-18G>A rs7157087 0.04825
NM_000257.4(MYH7):c.1605A>G (p.Glu535=) rs2069543 0.03319
NM_000257.4(MYH7):c.895+17G>A rs45580436 0.02377
NM_000257.4(MYH7):c.975C>T (p.Asp325=) rs2231124 0.01865
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781 0.01418
NM_000257.4(MYH7):c.1767C>T (p.Asn589=) rs3729816 0.01311
NM_000257.4(MYH7):c.3972+15C>T rs3729820 0.01159
NM_000257.4(MYH7):c.597A>G (p.Ala199=) rs2069541 0.00853
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831 0.00505
NM_000257.4(MYH7):c.1579-17C>T rs182949516 0.00470
NM_000257.4(MYH7):c.3864C>G (p.Ser1288=) rs45501694 0.00469
NM_000257.4(MYH7):c.3972+16G>A rs114978322 0.00424
NM_000257.4(MYH7):c.2162+4G>A rs145738465 0.00276
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821 0.00267
NM_000257.4(MYH7):c.3853+7C>T rs45467397 0.00247
NM_000257.4(MYH7):c.297C>T (p.Pro99=) rs140245862 0.00220
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=) rs45554236 0.00217
NM_000257.4(MYH7):c.-62C>T rs45566639 0.00185
NM_000257.4(MYH7):c.480C>T (p.Asn160=) rs45500700 0.00178
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355 0.00091
NM_000257.4(MYH7):c.1395C>T (p.Phe465=) rs45508293 0.00082
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=) rs144465613 0.00064
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643 0.00063
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716 0.00060
NM_000257.4(MYH7):c.2163-16A>T rs199538267 0.00055
NM_000257.4(MYH7):c.3777C>T (p.His1259=) rs149103761 0.00054
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951 0.00050
NM_000257.4(MYH7):c.2907C>T (p.His969=) rs142573531 0.00049
NM_000257.4(MYH7):c.3690C>T (p.Asp1230=) rs370750044 0.00038
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313 0.00030
NM_000257.4(MYH7):c.5725C>A (p.Arg1909=) rs146796870 0.00029
NM_000257.4(MYH7):c.2045-20C>A rs773185645 0.00025
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570 0.00021
NM_000257.4(MYH7):c.84C>G (p.Thr28=) rs200930470 0.00021
NM_000257.4(MYH7):c.3727-18C>T rs369549958 0.00016
NM_000257.4(MYH7):c.1407T>C (p.Asp469=) rs112172952 0.00008
NM_000257.4(MYH7):c.474C>T (p.Ser158=) rs200444892 0.00006
NM_000257.4(MYH7):c.1332T>C (p.Asn444=) rs397516099 0.00004
NM_000257.4(MYH7):c.4134C>T (p.Asp1378=) rs770630028 0.00002
NM_000257.4(MYH7):c.5484C>T (p.Ala1828=) rs202175645 0.00002
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597 0.00002
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362 0.00001
NM_000257.4(MYH7):c.1301G>A (p.Arg434Lys) rs786205356 0.00001
NM_000257.4(MYH7):c.797-17T>C rs532401716 0.00001
NM_000257.4(MYH7):c.3315G>A (p.Gln1105=)
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.3715A>G (p.Ile1239Val) rs1114167342
NM_000257.4(MYH7):c.396G>T (p.Pro132=) rs138932714
NM_000257.4(MYH7):c.3973-8dup rs762851416
NM_000257.4(MYH7):c.5451G>A (p.Ala1817=) rs138682220
NM_000257.4(MYH7):c.5560-7dup rs762612534
NM_000257.4(MYH7):c.896-8del rs781117720

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