ClinVar Miner

List of variants in gene MYH9 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_002473.5(MYH9):c.*1204A>T rs56360445
NM_002473.5(MYH9):c.*1329C>T rs146582828
NM_002473.5(MYH9):c.*1394C>T rs144335048
NM_002473.5(MYH9):c.*1399C>T rs544966086
NM_002473.5(MYH9):c.*243C>T rs136201
NM_002473.5(MYH9):c.*329C>T rs566336121
NM_002473.5(MYH9):c.*645C>G rs527539496
NM_002473.5(MYH9):c.*686C>T rs55994070
NM_002473.5(MYH9):c.*748A>G rs568025076
NM_002473.5(MYH9):c.*802T>G rs528245823
NM_002473.5(MYH9):c.*81C>T rs56134611
NM_002473.5(MYH9):c.*8C>T rs201455315
NM_002473.5(MYH9):c.*906G>T rs192511111
NM_002473.5(MYH9):c.-19-7C>T rs184332718
NM_002473.5(MYH9):c.1083C>T (p.Asp361=) rs56001030
NM_002473.5(MYH9):c.1098C>T (p.Pro366=) rs537679678
NM_002473.5(MYH9):c.1108+9C>T rs145751072
NM_002473.5(MYH9):c.1158C>T (p.Thr386=) rs138502859
NM_002473.5(MYH9):c.1176G>A (p.Pro392=) rs143316848
NM_002473.5(MYH9):c.1344C>T (p.Ile448=) rs150125254
NM_002473.5(MYH9):c.136C>T (p.Leu46Phe) rs147122501
NM_002473.5(MYH9):c.1479G>A (p.Gln493=) rs376262583
NM_002473.5(MYH9):c.1578C>G (p.Ala526=) rs201827299
NM_002473.5(MYH9):c.1626C>T (p.Phe542=) rs7285745
NM_002473.5(MYH9):c.1729-6C>T rs9622375
NM_002473.5(MYH9):c.18C>T (p.Ala6=) rs141055332
NM_002473.5(MYH9):c.2038-5T>C rs8137674
NM_002473.5(MYH9):c.2061C>T (p.Leu687=) rs143801000
NM_002473.5(MYH9):c.2205C>T (p.Asp735=) rs370860479
NM_002473.5(MYH9):c.2295C>T (p.Ala765=) rs150133983
NM_002473.5(MYH9):c.233C>T (p.Pro78Leu) rs150313549
NM_002473.5(MYH9):c.2448C>T (p.Cys816=) rs113285582
NM_002473.5(MYH9):c.2500-14A>G rs199505086
NM_002473.5(MYH9):c.2517G>A (p.Gln839=) rs34498733
NM_002473.5(MYH9):c.2635A>C (p.Met879Leu) rs200328859
NM_002473.5(MYH9):c.2721C>T (p.Thr907=) rs148112044
NM_002473.5(MYH9):c.2872G>A (p.Ala958Thr) rs151036570
NM_002473.5(MYH9):c.318C>T (p.Tyr106=) rs202117532
NM_002473.5(MYH9):c.3192C>T (p.Ile1064=) rs144807538
NM_002473.5(MYH9):c.3216G>A (p.Ala1072=) rs139441456
NM_002473.5(MYH9):c.3320G>A (p.Arg1107Gln) rs137924205
NM_002473.5(MYH9):c.3340T>C (p.Ser1114Pro) rs200901330
NM_002473.5(MYH9):c.3606G>A (p.Ala1202=) rs771461880
NM_002473.5(MYH9):c.3838-12C>T rs113698937
NM_002473.5(MYH9):c.3915G>A (p.Ala1305=) rs183685723
NM_002473.5(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635
NM_002473.5(MYH9):c.4225G>A (p.Asp1409Asn) rs34292387
NM_002473.5(MYH9):c.4344+10C>T rs200977419
NM_002473.5(MYH9):c.4359G>A (p.Glu1453=) rs202127454
NM_002473.5(MYH9):c.4391G>A (p.Arg1464His) rs199968414
NM_002473.5(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727
NM_002473.5(MYH9):c.4727G>A (p.Arg1576Gln) rs143269195
NM_002473.5(MYH9):c.4818G>A (p.Ser1606=) rs202132383
NM_002473.5(MYH9):c.4878C>T (p.Ile1626=) rs143947828
NM_002473.5(MYH9):c.4952T>C (p.Met1651Thr) rs142094977
NM_002473.5(MYH9):c.4955G>A (p.Arg1652His) rs779135945
NM_002473.5(MYH9):c.5010G>A (p.Glu1670=) rs76069100
NM_002473.5(MYH9):c.5143G>A (p.Gly1715Ser) rs148109368
NM_002473.5(MYH9):c.5323A>G (p.Lys1775Glu) rs145139708
NM_002473.5(MYH9):c.543G>A (p.Thr181=) rs146514663
NM_002473.5(MYH9):c.5483+4C>G rs56327920
NM_002473.5(MYH9):c.5765+9C>T rs201008102
NM_002473.5(MYH9):c.5818G>A (p.Gly1940Arg) rs140588099
NM_002473.5(MYH9):c.5877C>T (p.Ala1959=) rs144179406
NM_002473.5(MYH9):c.705+11C>T rs201738304
NM_002473.5(MYH9):c.705+14C>T rs142552338
NM_002473.5(MYH9):c.769+15C>T rs201691359
NM_002473.5(MYH9):c.7C>G (p.Gln3Glu) rs56200894
NM_002473.5(MYH9):c.933C>T (p.Pro311=) rs202045249

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