ClinVar Miner

List of variants in gene MYH6 reported as benign by Ambry Genetics

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.3302T>C (p.Val1101Ala) rs365990 0.44987
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.5259C>T (p.Ala1753=) rs8004990 0.07782
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.2579G>A (p.Arg860His) rs115845031 0.00573
NM_002471.4(MYH6):c.5475G>A (p.Glu1825=) rs79143968 0.00344
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile) rs148915045 0.00284
NM_002471.4(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550 0.00217
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.5439G>A (p.Gln1813=) rs200854143 0.00002
NM_002471.4(MYH6):c.3609C>G (p.Ala1203=) rs149369904

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