ClinVar Miner

List of variants in gene combination MYH2, MYHAS reported as uncertain significance by Illumina Laboratory Services, Illumina

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_017534.6(MYH2):c.3181C>G (p.Leu1061Val) rs142586585 0.00225
NM_017534.6(MYH2):c.87T>C (p.Asn29=) rs148217318 0.00050
NM_017534.6(MYH2):c.3128C>T (p.Ser1043Phe) rs200217946 0.00026
NM_017534.6(MYH2):c.2626A>G (p.Arg876Gly) rs201784718 0.00016
NM_017534.6(MYH2):c.-34C>T rs573601098 0.00014
NM_017534.6(MYH2):c.205-3C>T rs371123671 0.00008
NM_017534.6(MYH2):c.4149G>A (p.Thr1383=) rs376738763 0.00008
NM_017534.6(MYH2):c.1227C>T (p.Val409=) rs563146441 0.00006
NM_017534.6(MYH2):c.3709C>T (p.Leu1237Phe) rs138265883 0.00006
NM_017534.6(MYH2):c.4110C>T (p.Ala1370=) rs377674160 0.00005
NM_017534.6(MYH2):c.-60T>C rs886052575 0.00003
NM_017534.6(MYH2):c.1416+9G>A rs753547111 0.00003
NM_017534.6(MYH2):c.2655G>A (p.Thr885=) rs141764966 0.00003
NM_017534.6(MYH2):c.3489T>C (p.Thr1163=) rs780067831 0.00003
NM_017534.6(MYH2):c.2725G>T (p.Glu909Ter) rs780124402 0.00002
NM_017534.6(MYH2):c.3299T>C (p.Ile1100Thr) rs769463886 0.00002
NM_017534.6(MYH2):c.4205G>A (p.Arg1402Gln) rs781252325 0.00002
NM_017534.6(MYH2):c.5744G>A (p.Arg1915Gln) rs201882457 0.00002
NM_017534.6(MYH2):c.*131T>C rs1407636374 0.00001
NM_017534.6(MYH2):c.122C>T (p.Ala41Val) rs765877777 0.00001
NM_017534.6(MYH2):c.1251C>A (p.Gly417=) rs746987085 0.00001
NM_017534.6(MYH2):c.1711G>A (p.Val571Met) rs778226679 0.00001
NM_017534.6(MYH2):c.2305-11T>G rs369500791 0.00001
NM_017534.6(MYH2):c.2468A>G (p.Asn823Ser) rs1378547305 0.00001
NM_017534.6(MYH2):c.2654C>T (p.Thr885Met) rs150566222 0.00001
NM_017534.6(MYH2):c.3263+11A>G rs890845570 0.00001
NM_017534.6(MYH2):c.3358C>T (p.Arg1120Cys) rs756255059 0.00001
NM_017534.6(MYH2):c.3567A>G (p.Leu1189=) rs886052565 0.00001
NM_017534.6(MYH2):c.3839C>T (p.Thr1280Ile) rs886052564 0.00001
NM_017534.6(MYH2):c.4158C>A (p.Ile1386=) rs778626880 0.00001
NM_017534.6(MYH2):c.5294T>A (p.Ile1765Asn) rs139621607 0.00001
NM_017534.6(MYH2):c.-10T>C rs886052574
NM_017534.6(MYH2):c.-64+13A>G rs886052576
NM_017534.6(MYH2):c.1068G>A (p.Thr356=) rs116419997
NM_017534.6(MYH2):c.132A>C (p.Lys44Asn) rs2073654641
NM_017534.6(MYH2):c.1444A>C (p.Asn482His) rs886052570
NM_017534.6(MYH2):c.1644C>A (p.Asp548Glu) rs886052569
NM_017534.6(MYH2):c.1913G>A (p.Gly638Glu) rs2073484495
NM_017534.6(MYH2):c.2125C>T (p.Arg709Cys) rs761461325
NM_017534.6(MYH2):c.2181-9C>T rs886052568
NM_017534.6(MYH2):c.2264T>C (p.Ile755Thr) rs1167250510
NM_017534.6(MYH2):c.2331G>A (p.Gly777=) rs886052567
NM_017534.6(MYH2):c.2331G>T (p.Gly777=) rs886052567
NM_017534.6(MYH2):c.2396G>C (p.Arg799Thr) rs754150715
NM_017534.6(MYH2):c.2478C>T (p.Ser826=) rs2073428153
NM_017534.6(MYH2):c.2893C>T (p.Leu965=) rs886052566
NM_017534.6(MYH2):c.301G>C (p.Ala101Pro) rs886052573
NM_017534.6(MYH2):c.3263+12_3263+15del rs573872374
NM_017534.6(MYH2):c.3312G>A (p.Gln1104=) rs1257247271
NM_017534.6(MYH2):c.3369G>C (p.Glu1123Asp) rs2073391277
NM_017534.6(MYH2):c.3468G>A (p.Leu1156=) rs2073389597
NM_017534.6(MYH2):c.4007C>T (p.Ala1336Val) rs138470281
NM_017534.6(MYH2):c.4048C>T (p.Arg1350Trp) rs776018379
NM_017534.6(MYH2):c.495C>A (p.Phe165Leu) rs886052572
NM_017534.6(MYH2):c.5176-10T>C rs886052563
NM_017534.6(MYH2):c.5176-12C>A rs1270961978
NM_017534.6(MYH2):c.5616T>C (p.Asp1872=) rs2073304426
NM_017534.6(MYH2):c.71G>T (p.Arg24Leu) rs141174023

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