ClinVar Miner

List of variants in gene combination LOC114827851, MYH6 reported as likely benign for cardiomyopathy

Included ClinVar conditions (522):
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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.36G>A (p.Ala12=) rs141014719 0.00487
NM_002471.4(MYH6):c.531-19T>A rs374174532 0.00045
NM_002471.4(MYH6):c.408C>T (p.Ala136=) rs140732380 0.00024
NM_002471.4(MYH6):c.202-12C>T rs566157802 0.00020
NM_002471.4(MYH6):c.67C>T (p.Arg23Cys) rs587782959 0.00016
NM_002471.4(MYH6):c.115G>A (p.Val39Met) rs142850511 0.00012
NM_002471.4(MYH6):c.642+17A>G rs1458453275 0.00011
NM_002471.4(MYH6):c.420C>T (p.Ala140=) rs145023897 0.00010
NM_002471.4(MYH6):c.201+9G>A rs781068852 0.00006
NM_002471.4(MYH6):c.291C>T (p.His97=) rs144535842 0.00004
NM_002471.4(MYH6):c.297C>T (p.Pro99=) rs751088892 0.00004
NM_002471.4(MYH6):c.345+18A>G rs781746086 0.00004
NM_002471.4(MYH6):c.201+19C>T rs371665550 0.00003
NM_002471.4(MYH6):c.636G>A (p.Ala212=) rs111265123 0.00003
NM_002471.4(MYH6):c.189C>T (p.Thr63=) rs758633104 0.00002
NM_002471.4(MYH6):c.201+17G>A rs374935099 0.00002
NM_002471.4(MYH6):c.201+20G>A rs759225988 0.00002
NM_002471.4(MYH6):c.354G>A (p.Ser118=) rs373427673 0.00002
NM_002471.4(MYH6):c.453G>A (p.Pro151=) rs777360238 0.00002
NM_002471.4(MYH6):c.480C>T (p.Asn160=) rs780910329 0.00002
NM_002471.4(MYH6):c.530+7G>A rs1226127637 0.00002
NM_002471.4(MYH6):c.114C>T (p.Phe38=) rs777057620 0.00001
NM_002471.4(MYH6):c.177C>T (p.Val59=) rs1405820695 0.00001
NM_002471.4(MYH6):c.252C>T (p.Phe84=) rs397516757 0.00001
NM_002471.4(MYH6):c.333C>A (p.Ala111=) rs774402902 0.00001
NM_002471.4(MYH6):c.396G>A (p.Pro132=) rs369139462 0.00001
NM_002471.4(MYH6):c.503-15T>C rs1891742494 0.00001
NM_002471.4(MYH6):c.503-16C>T rs767894949 0.00001
NM_002471.4(MYH6):c.531-6C>T rs755395894 0.00001
NM_002471.4(MYH6):c.540C>T (p.Ser180=) rs766589542 0.00001
NM_002471.4(MYH6):c.627T>C (p.Asn209=) rs751659257 0.00001
NM_002471.4(MYH6):c.6C>T (p.Thr2=) rs770253223 0.00001
NM_002471.4(MYH6):c.105T>C (p.Thr35=) rs1345462210
NM_002471.4(MYH6):c.165G>A (p.Glu55=)
NM_002471.4(MYH6):c.201+10dup
NM_002471.4(MYH6):c.202-10C>T
NM_002471.4(MYH6):c.202-11G>A rs374248120
NM_002471.4(MYH6):c.202-11G>T
NM_002471.4(MYH6):c.202-14T>C rs2138620648
NM_002471.4(MYH6):c.245C>T (p.Pro82Leu) rs529427223
NM_002471.4(MYH6):c.300G>A (p.Ala100=) rs200520512
NM_002471.4(MYH6):c.318G>A (p.Lys106=) rs906582738
NM_002471.4(MYH6):c.321G>A (p.Glu107=) rs765093721
NM_002471.4(MYH6):c.324C>A (p.Arg108=)
NM_002471.4(MYH6):c.327C>T (p.Tyr109=)
NM_002471.4(MYH6):c.333C>T (p.Ala111=) rs774402902
NM_002471.4(MYH6):c.346-15T>C rs773519707
NM_002471.4(MYH6):c.474C>T (p.Ser158=) rs755939165
NM_002471.4(MYH6):c.483C>T (p.Ala161=)
NM_002471.4(MYH6):c.502+16C>T rs2138619637
NM_002471.4(MYH6):c.503-4C>T rs2138619457
NM_002471.4(MYH6):c.503-8T>C rs1566516373
NM_002471.4(MYH6):c.530+15T>G rs771353936
NM_002471.4(MYH6):c.546G>A (p.Ala182=) rs150015506
NM_002471.4(MYH6):c.546G>C (p.Ala182=)
NM_002471.4(MYH6):c.555T>C (p.Thr185=) rs761493890
NM_002471.4(MYH6):c.597A>G (p.Ala199=)
NM_002471.4(MYH6):c.636G>T (p.Ala212=) rs111265123
NM_002471.4(MYH6):c.639C>T (p.Asn213=)
NM_002471.4(MYH6):c.642+7T>C rs1595064042
NM_002471.4(MYH6):c.6C>G (p.Thr2=) rs770253223

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