ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "pathogenic" from Forensic Genetics Laboratory,Harris County Institute of Forensic Sciences

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: 3
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HGVS dbSNP
NM_000256.3(MYBPC3):c.13G>C (p.Gly5Arg) rs201278114
NM_000335.5(SCN5A):c.1844G>A (p.Gly615Glu) rs12720452
NM_001035.3(RYR2):c.3320C>T (p.Thr1107Met) rs200236750

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