ClinVar Miner

List of variants reported as uncertain significance by Institute of Reproductive and Stem Cell Engineering, Central South University

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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
NM_001370.2(DNAH6):c.11258G>A (p.Gly3753Asp)	rs1678342034
NM_001370.2(DNAH6):c.6582C>A (p.Asp2194Glu)	rs1692826738

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