ClinVar Miner

Submissions for variant NM_001719.3(BMP7):c.847G>A (p.Ala283Thr)

gnomAD frequency: 0.00004  dbSNP: rs560540219
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cytogenetics- Mohapatra Lab, Banaras Hindu University RCV002279854 SCV002567821 benign Tetralogy of Fallot no assertion criteria provided case-control

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