ClinVar Miner

Variants in gene LTBP4 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 22
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HGVS dbSNP
NM_001042545.2(LTBP4):c.135C>T (p.Cys45=) rs185400394
NM_003573.2(LTBP4):c.1328G>A (p.Gly443Asp) rs114749335
NM_003573.2(LTBP4):c.1390T>A (p.Ser464Thr) rs34545902
NM_003573.2(LTBP4):c.1531A>G (p.Met511Val) rs116005784
NM_003573.2(LTBP4):c.1581G>T (p.Arg527=) rs117273116
NM_003573.2(LTBP4):c.1792C>G (p.Arg598Gly) rs33937741
NM_003573.2(LTBP4):c.1924C>G (p.Pro642Ala) rs34299942
NM_003573.2(LTBP4):c.2143G>A (p.Asp715Asn) rs34093919
NM_003573.2(LTBP4):c.2144-11C>A rs41470347
NM_003573.2(LTBP4):c.2265C>T (p.Cys755=) rs141810975
NM_003573.2(LTBP4):c.2328C>T (p.Pro776=) rs201588216
NM_003573.2(LTBP4):c.2389+9A>G rs73544980
NM_003573.2(LTBP4):c.2526G>A (p.Val842=) rs371083223
NM_003573.2(LTBP4):c.2541G>A (p.Glu847=) rs191216887
NM_003573.2(LTBP4):c.2655C>T (p.Asp885=) rs2077407
NM_003573.2(LTBP4):c.3219C>T (p.Val1073=) rs78745792
NM_003573.2(LTBP4):c.3349G>A (p.Val1117Ile) rs369582949
NM_003573.2(LTBP4):c.4298G>A (p.Arg1433His)
NM_003573.2(LTBP4):c.4388A>T (p.Tyr1463Phe) rs35809725
NM_003573.2(LTBP4):c.79C>T (p.Leu27=) rs370696272
NM_003573.2(LTBP4):c.948G>A (p.Gly316=) rs146234365
NM_003573.2(LTBP4):c.981C>T (p.Gly327=) rs374427407

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