ClinVar Miner

List of variants in gene IVD reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002225.5(IVD):c.234+14T>C rs2289331 0.62561
NM_002225.5(IVD):c.*2275T>C rs11790 0.59170
NM_002225.5(IVD):c.*1471G>A rs4923865 0.56828
NM_002225.5(IVD):c.*1577C>G rs11630850 0.47386
NM_002225.5(IVD):c.*808C>G rs2075625 0.45103
NM_002225.5(IVD):c.*2844T>C rs7207 0.45094
NM_002225.5(IVD):c.*1610C>T rs11630878 0.44933
NM_002225.5(IVD):c.*261G>A rs2075624 0.23369
NM_002225.5(IVD):c.723C>T (p.Asp241=) rs2229312 0.11757
NM_002225.5(IVD):c.*2912G>A rs11557072 0.08940
NM_002225.5(IVD):c.*596G>A rs115034694 0.02695
NM_002225.5(IVD):c.*195C>T rs77680513 0.02693
NM_002225.5(IVD):c.*447C>G rs79191320 0.02689
NM_002225.5(IVD):c.1066-5C>T rs115077254 0.02192
NM_002225.5(IVD):c.*14C>T rs8040294 0.02023
NM_002225.5(IVD):c.*1208G>A rs7165233 0.01462
NM_002225.5(IVD):c.*2285C>G rs114657778 0.01453
NM_002225.5(IVD):c.88C>T (p.His30Tyr) rs73383128 0.00938
NM_002225.5(IVD):c.*2070C>T rs187887699 0.00062
NM_002225.5(IVD):c.*1890G>C rs12185076
NM_002225.5(IVD):c.*1893del rs398026948
NM_002225.5(IVD):c.*3036del rs5812161
NM_002225.5(IVD):c.*825C>A rs7182052

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