ClinVar Miner

Variants with conflicting interpretations "likely benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "likely pathogenic" from any submitter

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: 9
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HGVS dbSNP
NM_000059.4(BRCA2):c.831T>G (p.Asn277Lys) rs28897705
NM_000170.2(GLDC):c.1705G>A (p.Ala569Thr) rs151268759
NM_000243.2(MEFV):c.910G>A (p.Gly304Arg) rs75977701
NM_000243.3(MEFV):c.1105C>T rs11466023
NM_000243.3(MEFV):c.1223G>A rs11466024
NM_001148.6(ANK2):c.8324A>G (p.His2775Arg) rs534934297
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala) rs191564916
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys) rs576404380
NM_002878.3(RAD51D):c.796C>T (p.Arg266Cys) rs587781813

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