ClinVar Miner

List of variants in gene combination MYH2, MYHAS reported as uncertain significance by GeneDx

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_017534.6(MYH2):c.2270T>C (p.Ile757Thr) rs117390537 0.00103
NM_017534.6(MYH2):c.3308A>T (p.Glu1103Val) rs139295564 0.00085
NM_017534.6(MYH2):c.3884G>A (p.Arg1295His) rs143341678 0.00063
NM_017534.6(MYH2):c.2823G>T (p.Glu941Asp) rs138206136 0.00053
NM_017534.6(MYH2):c.332C>T (p.Ala111Val) rs140468333 0.00040
NM_017534.6(MYH2):c.878C>T (p.Thr293Ile) rs774544504 0.00031
NM_017534.6(MYH2):c.3820C>T (p.Arg1274Trp) rs191102801 0.00029
NM_017534.6(MYH2):c.1729G>A (p.Glu577Lys) rs564509544 0.00018
NM_017534.6(MYH2):c.3728C>T (p.Thr1243Met) rs150829316 0.00017
NM_017534.6(MYH2):c.3854G>A (p.Arg1285His) rs148326504 0.00017
NM_017534.6(MYH2):c.2626A>G (p.Arg876Gly) rs201784718 0.00016
NM_017534.6(MYH2):c.3029A>G (p.Gln1010Arg) rs148961199 0.00016
NM_017534.6(MYH2):c.1174A>G (p.Ser392Gly) rs139212712 0.00013
NM_017534.6(MYH2):c.2565G>A (p.Met855Ile) rs184494954 0.00011
NM_017534.6(MYH2):c.5263C>T (p.Arg1755Cys) rs202006788 0.00008
NM_017534.6(MYH2):c.3709C>T (p.Leu1237Phe) rs138265883 0.00006
NM_017534.6(MYH2):c.41C>T (p.Ala14Val) rs770499680 0.00006
NM_017534.6(MYH2):c.4213G>T (p.Ala1405Ser) rs199632177 0.00006
NM_017534.6(MYH2):c.3425G>A (p.Arg1142His) rs781136210 0.00005
NM_017534.6(MYH2):c.5282C>T (p.Ala1761Val) rs377385495 0.00005
NM_017534.6(MYH2):c.5580G>A (p.Thr1860=) rs761795343 0.00004
NM_017534.6(MYH2):c.5791C>T (p.Arg1931Trp) rs544066673 0.00004
NM_017534.6(MYH2):c.2378G>A (p.Arg793Gln) rs578188627 0.00003
NM_017534.6(MYH2):c.5476C>T (p.Arg1826Trp) rs755265718 0.00003
NM_017534.6(MYH2):c.182C>T (p.Thr61Met) rs145979297 0.00002
NM_017534.6(MYH2):c.105A>C (p.Lys35Asn) rs774068547 0.00001
NM_017534.6(MYH2):c.151A>G (p.Thr51Ala) rs190103324 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.3176G>A (p.Arg1059Lys) rs371178030 0.00001
NM_017534.6(MYH2):c.3767G>A (p.Arg1256Gln) rs141448415 0.00001
NM_017534.6(MYH2):c.5472+1G>A rs758888662 0.00001
NM_017534.6(MYH2):c.5566C>T (p.Leu1856Phe) rs1488236141 0.00001
NM_017534.6(MYH2):c.5707C>T (p.Arg1903Cys) rs777766586 0.00001
NM_017534.6(MYH2):c.5737G>A (p.Glu1913Lys) rs1350545511 0.00001
NM_017534.6(MYH2):c.1068G>C (p.Thr356=) rs116419997
NM_017534.6(MYH2):c.121G>A (p.Ala41Thr) rs2142325523
NM_017534.6(MYH2):c.1334G>T (p.Arg445Leu) rs201040489
NM_017534.6(MYH2):c.139T>C (p.Phe47Leu)
NM_017534.6(MYH2):c.1528G>A (p.Glu510Lys) rs772963819
NM_017534.6(MYH2):c.1762G>T (p.Val588Phe) rs1348155208
NM_017534.6(MYH2):c.2264T>C (p.Ile755Thr) rs1167250510
NM_017534.6(MYH2):c.2329G>T (p.Gly777Trp) rs2142305536
NM_017534.6(MYH2):c.2821G>A (p.Glu941Lys)
NM_017534.6(MYH2):c.2998A>G (p.Lys1000Glu)
NM_017534.6(MYH2):c.304G>A (p.Val102Met) rs1131691454
NM_017534.6(MYH2):c.3212C>T (p.Ser1071Phe) rs2142299853
NM_017534.6(MYH2):c.3635A>G (p.Gln1212Arg) rs1456213666
NM_017534.6(MYH2):c.3720T>A (p.Asn1240Lys)
NM_017534.6(MYH2):c.3739G>A (p.Ala1247Thr)
NM_017534.6(MYH2):c.3744G>C (p.Lys1248Asn)
NM_017534.6(MYH2):c.388A>G (p.Lys130Glu)
NM_017534.6(MYH2):c.4027C>T (p.Arg1343Cys) rs145911509
NM_017534.6(MYH2):c.4033G>A (p.Asp1345Asn)
NM_017534.6(MYH2):c.4184C>A (p.Ala1395Asp) rs2142295252
NM_017534.6(MYH2):c.4222G>A (p.Glu1408Lys) rs780588979
NM_017534.6(MYH2):c.491A>C (p.Gln164Pro)
NM_017534.6(MYH2):c.5171C>G (p.Thr1724Ser) rs202050465
NM_017534.6(MYH2):c.5332G>A (p.Glu1778Lys)
NM_017534.6(MYH2):c.5429C>T (p.Ala1810Val)
NM_017534.6(MYH2):c.5749G>A (p.Asp1917Asn) rs1051054791

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