ClinVar Miner

List of variants in gene ABCC9 reported as likely benign for Dilated cardiomyopathy 1O

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Gene type:
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Total variants: 33
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HGVS dbSNP
NM_005691.3(ABCC9):c.1011+7T>C rs1224367944
NM_005691.3(ABCC9):c.1165-5G>T rs1411076886
NM_005691.3(ABCC9):c.1212C>T (p.Ser404=) rs376726505
NM_005691.3(ABCC9):c.1296C>T (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1332C>T (p.Gly444=) rs369830406
NM_005691.3(ABCC9):c.133T>C (p.Leu45=) rs1555125400
NM_005691.3(ABCC9):c.1416T>C (p.Phe472=) rs777308898
NM_005691.3(ABCC9):c.1524T>C (p.Tyr508=) rs1555112390
NM_005691.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1619-7T>C rs769816456
NM_005691.3(ABCC9):c.1785A>G (p.Ala595=) rs1555106091
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2154C>T (p.Ile718=) rs74067815
NM_005691.3(ABCC9):c.2157C>T (p.Leu719=) rs201848437
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.2574C>T (p.Phe858=) rs1273498300
NM_005691.3(ABCC9):c.2856C>T (p.Asp952=) rs758697683
NM_005691.3(ABCC9):c.2961A>G (p.Thr987=) rs1555187333
NM_005691.3(ABCC9):c.3316-4A>C rs201147809
NM_005691.3(ABCC9):c.3331T>C (p.Leu1111=) rs764155671
NM_005691.3(ABCC9):c.3621T>C (p.Ile1207=) rs767458242
NM_005691.3(ABCC9):c.3729G>A (p.Ser1243=) rs140182559
NM_005691.3(ABCC9):c.3993C>T (p.His1331=) rs377704379
NM_005691.3(ABCC9):c.3999G>A (p.Lys1333=) rs1555178738
NM_005691.3(ABCC9):c.4014T>C (p.Pro1338=) rs1555178731
NM_005691.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_005691.3(ABCC9):c.4344T>C (p.Asn1448=) rs146782703
NM_005691.3(ABCC9):c.4353T>C (p.Val1451=) rs771226136
NM_005691.3(ABCC9):c.4437T>C (p.Ile1479=) rs368079660
NM_005691.3(ABCC9):c.4497C>T (p.Thr1499=) rs1060504811
NM_005691.3(ABCC9):c.48C>T (p.Asn16=) rs199631710
NM_005691.3(ABCC9):c.817-14_817-4del rs774857795
NM_005691.3(ABCC9):c.837A>G (p.Pro279=) rs1264086698

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