ClinVar Miner

List of variants in gene MYH9 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_002473.5(MYH9):c.*1026C>G rs779365782
NM_002473.5(MYH9):c.*107A>G rs886057476
NM_002473.5(MYH9):c.*1099A>T rs886057471
NM_002473.5(MYH9):c.*1193A>G rs886057470
NM_002473.5(MYH9):c.*193C>T rs181364853
NM_002473.5(MYH9):c.*198dup rs886057475
NM_002473.5(MYH9):c.*474C>T rs55979529
NM_002473.5(MYH9):c.*539G>A rs533769148
NM_002473.5(MYH9):c.*656T>C rs886057474
NM_002473.5(MYH9):c.*74G>A rs886057477
NM_002473.5(MYH9):c.*975A>G rs886057473
NM_002473.5(MYH9):c.*978A>G rs886057472
NM_002473.5(MYH9):c.-153C>T rs886057485
NM_002473.5(MYH9):c.-163C>G rs886057486
NM_002473.5(MYH9):c.-182G>T rs868824019
NM_002473.5(MYH9):c.1150G>A (p.Asp384Asn) rs767088377
NM_002473.5(MYH9):c.1188G>A (p.Val396=) rs147972823
NM_002473.5(MYH9):c.132C>T (p.Ala44=) rs138526426
NM_002473.5(MYH9):c.1539C>A (p.Asp513Glu) rs886057484
NM_002473.5(MYH9):c.1730T>C (p.Val577Ala)
NM_002473.5(MYH9):c.1899C>T (p.Pro633=) rs749696998
NM_002473.5(MYH9):c.193G>A (p.Val65Met) rs377348805
NM_002473.5(MYH9):c.2226C>T (p.Leu742=) rs762499584
NM_002473.5(MYH9):c.2230-11C>A rs374467213
NM_002473.5(MYH9):c.2391-7C>T rs886057483
NM_002473.5(MYH9):c.2598C>G (p.Asn866Lys) rs750718366
NM_002473.5(MYH9):c.2632-8_2632-6del rs773975934
NM_002473.5(MYH9):c.2714G>A (p.Arg905His) rs727503289
NM_002473.5(MYH9):c.2761G>A (p.Glu921Lys)
NM_002473.5(MYH9):c.3136C>G (p.Leu1046Val) rs886057482
NM_002473.5(MYH9):c.3371G>A (p.Arg1124His) rs765237081
NM_002473.5(MYH9):c.3561C>A (p.Ile1187=) rs876657520
NM_002473.5(MYH9):c.3584C>T (p.Ser1195Leu)
NM_002473.5(MYH9):c.3605C>T (p.Ala1202Val) rs772915368
NM_002473.5(MYH9):c.3638C>G (p.Ala1213Gly) rs886057481
NM_002473.5(MYH9):c.3677G>A (p.Arg1226Gln) rs200697030
NM_002473.5(MYH9):c.3838-11G>A rs754547754
NM_002473.5(MYH9):c.3884A>G (p.Lys1295Arg) rs886057480
NM_002473.5(MYH9):c.4025G>A (p.Arg1342Gln) rs758159686
NM_002473.5(MYH9):c.4126A>G (p.Ser1376Gly) rs771692651
NM_002473.5(MYH9):c.420C>T (p.Gly140=) rs372621048
NM_002473.5(MYH9):c.4261G>A (p.Glu1421Lys)
NM_002473.5(MYH9):c.4262A>C (p.Glu1421Ala)
NM_002473.5(MYH9):c.4297C>T (p.Arg1433Cys) rs727503286
NM_002473.5(MYH9):c.4302G>C (p.Gln1434His)
NM_002473.5(MYH9):c.4305C>T (p.Ser1435=) rs768359816
NM_002473.5(MYH9):c.4345-11C>G rs376040199
NM_002473.5(MYH9):c.4348C>T (p.Leu1450=) rs764948348
NM_002473.5(MYH9):c.4474A>G (p.Lys1492Glu) rs750188842
NM_002473.5(MYH9):c.4654G>A (p.Glu1552Lys) rs886057479
NM_002473.5(MYH9):c.4830C>T (p.Ala1610=) rs751904301
NM_002473.5(MYH9):c.4946A>G (p.Asp1649Gly)
NM_002473.5(MYH9):c.4972C>T (p.Arg1658Cys) rs143972348
NM_002473.5(MYH9):c.5032A>G (p.Met1678Val)
NM_002473.5(MYH9):c.5050C>T (p.Gln1684Ter)
NM_002473.5(MYH9):c.5081G>A (p.Arg1694His)
NM_002473.5(MYH9):c.519-10del rs754795681
NM_002473.5(MYH9):c.5271G>T (p.Leu1757=) rs886057478
NM_002473.5(MYH9):c.5275-7_5275-5delTCT rs780656298
NM_002473.5(MYH9):c.5456T>G (p.Leu1819Arg) rs368440234
NM_002473.5(MYH9):c.5593-14G>A rs201676960
NM_002473.5(MYH9):c.5717C>T (p.Thr1906Met) rs149663189
NM_002473.5(MYH9):c.585G>A (p.Ala195=) rs374395918
NM_002473.5(MYH9):c.658G>A (p.Ala220Thr) rs1556637683

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