ClinVar Miner

List of variants in gene combination CBR4, PALLD reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.2623-30C>G rs1532651 0.76195
NM_001166108.2(PALLD):c.3358+26T>C rs3733656 0.68346
NM_001166108.2(PALLD):c.3058+84T>C rs17615157 0.52954
NM_001166108.2(PALLD):c.2717+152T>G rs4324524 0.52403
NM_001166108.2(PALLD):c.*2058C>G rs1071738 0.51499
NM_001166108.2(PALLD):c.2251-55G>A rs10026521 0.15466
NM_001166108.2(PALLD):c.3058+150A>T rs17054576 0.15231
NM_001166108.2(PALLD):c.3224+149C>T rs4396955 0.14742
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=) rs1059444 0.12743
NM_001166108.2(PALLD):c.*1906G>A rs1136603 0.12735
NM_001166108.2(PALLD):c.2718-85T>C rs72704235 0.08880
NM_001166108.2(PALLD):c.3359-4G>A rs112116419 0.01744
NM_001166108.2(PALLD):c.3058+28C>G rs114820369 0.00457
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00447
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=) rs59633770 0.00138
NM_001166108.2(PALLD):c.*2162ATCA[2] rs71719276
NM_001166108.2(PALLD):c.*325del rs796761323
NM_001166108.2(PALLD):c.*33-237del rs11357121
NM_001166108.2(PALLD):c.2199+277A>T rs10020879
NM_001166108.2(PALLD):c.2851-108del rs5863967
NM_001166108.2(PALLD):c.2851-108dup rs5863967
NM_001166108.2(PALLD):c.3359-24CT[5] rs536545858

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