ClinVar Miner

List of variants in gene LDB3 reported as benign for Cardiomyopathy

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.1074C>T (p.Ala358=) rs45459491 0.02721
NM_007078.3(LDB3):c.1903G>A (p.Val635Ile) rs45618633 0.01846
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg) rs34423165 0.01591
NM_007078.3(LDB3):c.609G>A (p.Ser203=) rs45531131 0.01451
NM_007078.3(LDB3):c.302C>T (p.Pro101Leu) rs45592139 0.00899
NM_007078.3(LDB3):c.1506G>A (p.Pro502=) rs45579241 0.00863
NM_007078.3(LDB3):c.1014A>G (p.Thr338=) rs150209221 0.00417
NM_007078.3(LDB3):c.690-4A>G rs45529531 0.00411
NM_007078.3(LDB3):c.352G>A (p.Val118Met) rs35507268 0.00408
NM_007078.3(LDB3):c.147G>A (p.Val49=) rs45591834 0.00312
NM_007078.3(LDB3):c.163G>A (p.Val55Ile) rs3740343 0.00292
NM_007078.3(LDB3):c.1535A>C (p.Gln512Pro) rs138951890 0.00068
NM_007078.3(LDB3):c.1956C>T (p.Asp652=) rs139213290 0.00014
NM_007078.3(LDB3):c.493C>T (p.Arg165Trp) rs45610637 0.00009
NM_007078.3(LDB3):c.1672A>G (p.Ile558Val) rs372331627 0.00003
NM_007078.3(LDB3):c.1041C>A (p.Ser347=) rs45555240
NM_007078.3(LDB3):c.1294T>C (p.Ser432Pro) rs768062879
NM_007078.3(LDB3):c.1296_1343del (p.Ala434_Pro449del) rs397517209
NM_007078.3(LDB3):c.1299T>C (p.Pro433=) rs761685061
NM_007078.3(LDB3):c.1300G>C (p.Ala434Pro) rs769720685
NM_007078.3(LDB3):c.1305T>C (p.Pro435=) rs1009984915
NM_007078.3(LDB3):c.1306G>C (p.Ala436Pro) rs1390883820
NM_007078.3(LDB3):c.576G>A (p.Pro192=) rs45543741
NM_007078.3(LDB3):c.576G>T (p.Pro192=) rs45543741

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