ClinVar Miner

List of variants in gene IVD reported as uncertain significance for not specified

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_002225.5(IVD):c.1124G>A (p.Gly375Asp) rs769261274 0.00004
NM_002225.5(IVD):c.1232G>A (p.Arg411Gln) rs143348838 0.00004
NM_002225.5(IVD):c.1123G>A (p.Gly375Ser) rs544110604 0.00002
NM_002225.5(IVD):c.596G>T (p.Gly199Val) rs121434285 0.00002
NM_002225.5(IVD):c.1132T>C (p.Cys378Arg) rs398123680 0.00001
NM_002225.5(IVD):c.1205T>C (p.Ile402Thr) rs763422682 0.00001
NM_002225.5(IVD):c.1065G>C (p.Lys355Asn) rs910454086
NM_002225.5(IVD):c.1138+3_1138+14del
NM_002225.5(IVD):c.380G>T (p.Gly127Val) rs1195537609
NM_002225.5(IVD):c.823G>A (p.Val275Met) rs757832700
NM_002225.5(IVD):c.860T>C (p.Leu287Pro)
NM_002225.5(IVD):c.889G>A (p.Ala297Thr) rs2141355228

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