ClinVar Miner

Variants with conflicting interpretations "likely benign" from Center for Advanced Laboratory Medicine, UC San Diego Health,University of California San Diego and "benign" from any submitter

Minimum review status of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health,University of California San Diego: Collection method of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health,University of California San Diego:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 18
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HGVS dbSNP
NM_000256.3(MYBPC3):c.3004C>T (p.Arg1002Trp) rs3729799
NM_000256.3(MYBPC3):c.3413G>A (p.Arg1138His) rs187705120
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001005242.3(PKP2):c.1379-2019C>T rs149930872
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001267550.2(TTN):c.104774A>C (p.Glu34925Ala) rs201218828
NM_001267550.2(TTN):c.17871A>T (p.Gln5957His) rs181067357
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu) rs73973139
NM_001267550.2(TTN):c.71705T>C (p.Ile23902Thr) rs55837610
NM_001267550.2(TTN):c.78892G>A (p.Gly26298Arg) rs72648205
NM_001267550.2(TTN):c.92176C>T (p.Pro30726Ser) rs72648247
NM_001267550.2(TTN):c.95582A>G (p.Tyr31861Cys) rs59148238
NM_001267550.2(TTN):c.97760G>A (p.Arg32587His) rs55704830
NM_004415.4(DSP):c.12C>G (p.Asn4Lys) rs368802003
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly) rs28763965
NM_017636.4(TRPM4):c.3611C>T (p.Pro1204Leu) rs150391806
NM_033118.4(MYLK2):c.173C>A (p.Ala58Asp) rs138130914
NM_033337.2(CAV3):c.216C>G (p.Cys72Trp) rs116840776

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