ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "likely pathogenic" from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology

Minimum review status of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp: Collection method of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_000053.4(ATP7B):c.2605G>A (p.Gly869Arg) rs191312027
NM_000303.3(PMM2):c.368G>A (p.Arg123Gln) rs141498002
NM_000492.4(CFTR):c.350G>A (p.Arg117His) rs78655421
NM_000527.5(LDLR):c.1747C>T (p.His583Tyr) rs730882109
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys) rs34612342

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