ClinVar Miner

Variants with conflicting interpretations "likely benign" from Center for Advanced Laboratory Medicine, UC San Diego Health,University of California San Diego and "uncertain significance" from CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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: 6
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HGVS dbSNP
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849
NM_001134363.3(RBM20):c.1286T>C (p.Leu429Pro) rs61735272
NM_001267550.2(TTN):c.29042-2A>C rs6716782
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly) rs147000526
NM_014000.3(VCL):c.590C>T (p.Thr197Ile) rs189242810

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