ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Department of Medical Genetics,Sanjay Gandhi Post Graduate Institute of Medical Sciences and "pathogenic" from any submitter

Minimum review status of the submission from Department of Medical Genetics,Sanjay Gandhi Post Graduate Institute of Medical Sciences: Collection method of the submission from Department of Medical Genetics,Sanjay Gandhi Post Graduate Institute of Medical Sciences:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP
NM_001080477.4(TENM3):c.4046C>G (p.Ala1349Gly) rs1243762658
NM_001080477.4(TENM3):c.7687C>T (p.Arg2563Trp) rs755000701

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