ClinVar Miner

List of variants in gene combination LOC130062794, TXNL4A reported as not provided for Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NC_000018.9(TXNL4A):g.77748604_77748637del34	rs786205699
NC_000018.9:g.77748581_77748614del34	rs535089924

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