ClinVar Miner

Variants in gene MYH9 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 91
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.3838-12C>T rs113698937 0.01529
NM_002473.6(MYH9):c.*243C>T rs136201 0.00965
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe) rs147122501 0.00554
NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr) rs115031369 0.00508
NM_002473.6(MYH9):c.1083C>T (p.Asp361=) rs56001030 0.00436
NM_002473.6(MYH9):c.1555-12C>T rs148641114 0.00392
NM_002473.6(MYH9):c.2229+13G>T rs139146113 0.00334
NM_002473.6(MYH9):c.5181G>A (p.Leu1727=) rs115170675 0.00292
NM_002473.6(MYH9):c.7C>G (p.Gln3Glu) rs56200894 0.00217
NM_002473.6(MYH9):c.5143G>A (p.Gly1715Ser) rs148109368 0.00198
NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727 0.00194
NM_002473.6(MYH9):c.165C>T (p.Ile55=) rs141948797 0.00187
NM_002473.6(MYH9):c.3485+8C>T rs149559551 0.00182
NM_002473.6(MYH9):c.4952T>C (p.Met1651Thr) rs142094977 0.00165
NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg) rs140588099 0.00147
NM_002473.6(MYH9):c.705+14C>T rs142552338 0.00136
NM_002473.6(MYH9):c.5323A>G (p.Lys1775Glu) rs145139708 0.00132
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635 0.00123
NM_002473.6(MYH9):c.1176G>A (p.Pro392=) rs143316848 0.00121
NM_002473.6(MYH9):c.1158C>T (p.Thr386=) rs138502859 0.00119
NM_002473.6(MYH9):c.705+11C>T rs201738304 0.00114
NM_002473.6(MYH9):c.2448C>T (p.Cys816=) rs113285582 0.00112
NM_002473.6(MYH9):c.1228-16C>T rs186815044 0.00106
NM_002473.6(MYH9):c.615C>T (p.Gly205=) rs139466141 0.00090
NM_002473.6(MYH9):c.5010G>A (p.Glu1670=) rs76069100 0.00088
NM_002473.6(MYH9):c.4727G>A (p.Arg1576Gln) rs143269195 0.00087
NM_002473.6(MYH9):c.1242C>T (p.Ile414=) rs138436678 0.00081
NM_002473.6(MYH9):c.2517G>A (p.Gln839=) rs34498733 0.00076
NM_002473.6(MYH9):c.3192C>T (p.Ile1064=) rs144807538 0.00076
NM_002473.6(MYH9):c.5049C>A (p.Ile1683=) rs147419066 0.00076
NM_002473.6(MYH9):c.1843+14C>A rs372865551 0.00072
NM_002473.6(MYH9):c.1728+47G>T rs201272453 0.00068
NM_002473.6(MYH9):c.5877C>T (p.Ala1959=) rs144179406 0.00066
NM_002473.6(MYH9):c.591G>A (p.Ser197=) rs140241271 0.00062
NM_002473.6(MYH9):c.4344+10C>T rs200977419 0.00061
NM_002473.6(MYH9):c.1566G>A (p.Pro522=) rs145517108 0.00057
NM_002473.6(MYH9):c.3216G>A (p.Ala1072=) rs139441456 0.00055
NM_002473.6(MYH9):c.3485+18G>C rs200835614 0.00046
NM_002473.6(MYH9):c.5026A>G (p.Lys1676Glu) rs138158369 0.00044
NM_002473.6(MYH9):c.769+15C>T rs201691359 0.00044
NM_002473.6(MYH9):c.4878C>T (p.Ile1626=) rs143947828 0.00041
NM_002473.6(MYH9):c.1167C>T (p.Ile389=) rs114048959 0.00036
NM_002473.6(MYH9):c.2500-14A>G rs199505086 0.00031
NM_002473.6(MYH9):c.4902C>T (p.Asp1634=) rs146184921 0.00030
NM_002473.6(MYH9):c.3195C>A (p.Ala1065=) rs148781875 0.00029
NM_002473.6(MYH9):c.1479G>A (p.Gln493=) rs376262583 0.00025
NM_002473.6(MYH9):c.2061C>T (p.Leu687=) rs143801000 0.00022
NM_002473.6(MYH9):c.4956C>T (p.Arg1652=) rs148632964 0.00022
NM_002473.6(MYH9):c.1098C>T (p.Pro366=) rs537679678 0.00020
NM_002473.6(MYH9):c.2295C>T (p.Ala765=) rs150133983 0.00018
NM_002473.6(MYH9):c.32A>G (p.Tyr11Cys) rs201415443 0.00015
NM_002473.6(MYH9):c.543G>A (p.Thr181=) rs146514663 0.00015
NM_002473.6(MYH9):c.5378A>G (p.Lys1793Arg) rs141440715 0.00014
NM_002473.6(MYH9):c.3214G>A (p.Ala1072Thr) rs532156048 0.00013
NM_002473.6(MYH9):c.3693C>T (p.Asn1231=) rs148043336 0.00012
NM_002473.6(MYH9):c.5709C>T (p.Ala1903=) rs145444485 0.00012
NM_002473.6(MYH9):c.1980G>A (p.Thr660=) rs200975323 0.00011
NM_002473.6(MYH9):c.5277C>T (p.Ile1759=) rs183105164 0.00011
NM_002473.6(MYH9):c.4008C>T (p.Asp1336=) rs373378393 0.00009
NM_002473.6(MYH9):c.5118G>A (p.Leu1706=) rs34849414 0.00008
NM_002473.6(MYH9):c.5742C>T (p.Val1914=) rs150728943 0.00008
NM_002473.6(MYH9):c.4345-11C>G rs376040199 0.00007
NM_002473.6(MYH9):c.5694C>T (p.Arg1898=) rs559732738 0.00007
NM_002473.6(MYH9):c.5787C>T (p.Val1929=) rs367698156 0.00007
NM_002473.6(MYH9):c.1578C>G (p.Ala526=) rs201827299 0.00006
NM_002473.6(MYH9):c.4203C>T (p.His1401=) rs539186034 0.00006
NM_002473.6(MYH9):c.5456T>G (p.Leu1819Arg) rs368440234 0.00006
NM_002473.6(MYH9):c.3039G>A (p.Glu1013=) rs755319033 0.00005
NM_002473.6(MYH9):c.3384T>C (p.Asn1128=) rs531623930 0.00005
NM_002473.6(MYH9):c.3915G>A (p.Ala1305=) rs183685723 0.00005
NM_002473.6(MYH9):c.5247C>T (p.Asn1749=) rs146848144 0.00005
NM_002473.6(MYH9):c.933C>T (p.Pro311=) rs202045249 0.00005
NM_002473.6(MYH9):c.1686G>A (p.Leu562=) rs199506577 0.00004
NM_002473.6(MYH9):c.3320G>A (p.Arg1107Gln) rs137924205 0.00004
NM_002473.6(MYH9):c.1899C>T (p.Pro633=) rs749696998 0.00003
NM_002473.6(MYH9):c.3453G>A (p.Thr1151=) rs574230328 0.00003
NM_002473.6(MYH9):c.468C>T (p.Thr156=) rs727503293 0.00003
NM_002473.6(MYH9):c.4830C>T (p.Ala1610=) rs751904301 0.00003
NM_002473.6(MYH9):c.5817C>T (p.Ala1939=) rs537608045 0.00003
NM_002473.6(MYH9):c.318C>T (p.Tyr106=) rs202117532 0.00002
NM_002473.6(MYH9):c.5829C>T (p.Ser1943=) rs750263908 0.00002
NM_002473.6(MYH9):c.5853G>A (p.Ala1951=) rs746116612 0.00002
NM_002473.6(MYH9):c.585G>A (p.Ala195=) rs374395918 0.00002
NM_002473.6(MYH9):c.1389G>A (p.Ser463=) rs757449139 0.00001
NM_002473.6(MYH9):c.153C>T (p.Gly51=) rs748117872 0.00001
NM_002473.6(MYH9):c.2977-10C>T rs188843586 0.00001
NM_002473.6(MYH9):c.3697G>A (p.Val1233Met) rs542791128 0.00001
NM_002473.6(MYH9):c.720C>T (p.Arg240=) rs556214390 0.00001
NM_002473.6(MYH9):c.3677G>T (p.Arg1226Leu) rs200697030
NM_002473.6(MYH9):c.5275-10del rs552643559
NM_002473.6(MYH9):c.5593-14G>T rs201676960

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