ClinVar Miner

Variants in gene NTRK1 with conflicting interpretations "pathogenic" and "pathogenic"

Submission 1 (pathogenic) minimum review status: Submission 1 (pathogenic) method:
Submission 2 (pathogenic) minimum review status: Submission 2 (pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 3
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NM_001007792.1(NTRK1):c.1552del (p.Arg518fs) rs80356675
NM_001007792.1(NTRK1):c.1752_1753insT (p.Pro585fs) rs80356676
NM_001007792.1(NTRK1):c.761-33T>A rs80356674

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