ClinVar Miner

List of variants in gene IVD reported as likely benign for not specified

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_002225.5(IVD):c.235-19T>C rs144063157 0.00186
NM_002225.5(IVD):c.11C>T (p.Ala4Val) rs148189323 0.00157
NM_002225.5(IVD):c.891G>A (p.Ala297=) rs138427412 0.00069
NM_002225.5(IVD):c.229C>T (p.Leu77=) rs143807229 0.00032
NM_002225.5(IVD):c.400A>G (p.Ile134Val) rs151118565 0.00026
NM_002225.5(IVD):c.234+16C>T rs750473075 0.00025
NM_002225.5(IVD):c.879-5G>A rs750569823 0.00014
NM_002225.5(IVD):c.961T>C (p.Leu321=) rs146011049 0.00011
NM_002225.5(IVD):c.784+13G>A rs369694967 0.00006
NM_002225.5(IVD):c.1122C>T (p.Asp374=) rs372504234 0.00005
NM_002225.5(IVD):c.1066-10C>T rs774472099 0.00003
NM_002225.5(IVD):c.1139-8G>C rs755640305 0.00003
NM_002225.5(IVD):c.264C>T (p.Gly88=) rs377199313 0.00003
NM_002225.3(IVD):c.-27C>T rs545229523 0.00001
NM_002225.5(IVD):c.123G>C (p.Gly41=) rs139179135 0.00001
NM_002225.5(IVD):c.150T>A (p.Arg50=) rs762440985 0.00001
NM_002225.5(IVD):c.690T>C (p.Gly230=) rs1182189552 0.00001
NM_002225.5(IVD):c.784+12C>T rs572858305 0.00001
NM_002225.5(IVD):c.948C>T (p.Ile316=) rs754100750 0.00001
NM_002225.5(IVD):c.234+17G>A rs568900608
NM_002225.5(IVD):c.286+16_286+17del rs775497134

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