ClinVar Miner

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

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: 4
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HGVS dbSNP
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829
NM_001267550.2(TTN):c.15178G>C (p.Val5060Leu) rs72648929
NM_003276.2(TMPO):c.1277C>T (p.Pro426Leu) rs141443652
NM_005751.4(AKAP9):c.11273G>A (p.Arg3758His) rs141856443

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