ClinVar Miner

List of variants studied for Cystic fibrosis; Congenital bilateral aplasia of vas deferens from CFTR mutation by GenomeConnect - Invitae Patient Insights Network

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000492.4(CFTR):c.3846G>A (p.Trp1282Ter) rs77010898 0.00019

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