ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1178-155A>G

gnomAD frequency: 0.00451  dbSNP: rs140550074
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002211118 SCV002496945 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing NTRK1: BS1
Breakthrough Genomics, Breakthrough Genomics RCV002211118 SCV005282806 benign not provided criteria provided, single submitter not provided

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