ClinVar Miner

List of variants in gene MYH6 reported as benign for not provided

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Gene type:
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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.800-11A>G rs434273 0.81807
NM_002471.4(MYH6):c.4526-34T>C rs178642 0.47911
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.1962+39T>C rs412768 0.35458
NM_002471.4(MYH6):c.1582-39C>T rs439735 0.22818
NM_002471.4(MYH6):c.5565+22A>G rs8006357 0.22619
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.5164-22A>G rs178637 0.07783
NM_002471.4(MYH6):c.5259C>T (p.Ala1753=) rs8004990 0.07782
NM_002471.4(MYH6):c.5566-8A>C rs529785746 0.04893
NM_002471.4(MYH6):c.1335C>T (p.Asn445=) rs61731179 0.03984
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.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.4206C>T (p.Ala1402=) rs111638554 0.00728
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.1003-29C>A rs45466392 0.00403
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.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.2928+5G>A rs28730772 0.00172
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala) rs142992009 0.00153
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.3303G>A (p.Val1101=) rs143825034 0.00095
NM_002471.4(MYH6):c.735+16C>T rs76202841 0.00080
NM_002471.4(MYH6):c.5652C>T (p.Ala1884=) rs200662317 0.00062
NM_002471.4(MYH6):c.3903G>A (p.Ser1301=) rs201804323 0.00052
NM_002471.4(MYH6):c.4293G>A (p.Met1431Ile) rs201016285 0.00029
NM_002471.4(MYH6):c.5439G>A (p.Gln1813=) rs200854143 0.00002
NC_000014.9:g.23409719C>A
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.3609C>G (p.Ala1203=) rs149369904
NM_002471.4(MYH6):c.3979-11C>G rs200618133
NM_002471.4(MYH6):c.3979-11_3979-9delinsG rs368229372
NM_002471.4(MYH6):c.3979-14C>A rs372226248
NM_002471.4(MYH6):c.3979-7T>C rs535111647
NM_002471.4(MYH6):c.3979-8C>T rs555976716
NM_002471.4(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.4(MYH6):c.3979-9C>A rs57660219
NM_002471.4(MYH6):c.4360-7C>T rs58949384

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