ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Fundacion Hipercolesterolemia Familiar and "uncertain significance" from any submitter

Minimum review status of the submission from Fundacion Hipercolesterolemia Familiar: Collection method of the submission from Fundacion Hipercolesterolemia Familiar:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP
NM_000527.4(LDLR):c.-120C>T rs875989886
NM_000527.5(LDLR):c.1247G>A (p.Arg416Gln) rs773658037
NM_000527.5(LDLR):c.1301C>G (p.Thr434Arg) rs745343524
NM_000527.5(LDLR):c.1796T>C (p.Leu599Ser) rs879255025
NM_000527.5(LDLR):c.337G>A (p.Glu113Lys) rs769383881
NM_000527.5(LDLR):c.862G>A (p.Glu288Lys) rs368657165
NM_000527.5(LDLR):c.898A>G (p.Arg300Gly) rs767618089
NM_000527.5(LDLR):c.974G>A (p.Cys325Tyr) rs879254746

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