ClinVar Miner

List of variants reported as likely pathogenic by 3DMed Clinical Laboratory Inc

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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NM_000059.3(BRCA2):c.82_147del (p.Leu29_Ser50del) rs1593882341
NM_004360.5(CDH1):c.1296C>G (p.Asn432Lys) rs187862045
NM_007294.4(BRCA1):c.5141T>G (p.Val1714Gly) rs80357243

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