ClinVar Miner

List of variants reported as benign for Neurodegeneration with brain iron accumulation 4

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_031448.6(C19orf12):c.*1686T>C rs7255131 0.78821
NM_031448.6(C19orf12):c.*2961T>C rs10417597 0.76596
NM_031448.6(C19orf12):c.*3096_*3097insG rs35973369 0.76181
NM_031448.6(C19orf12):c.*881G>A rs3926 0.73115
NM_031448.6(C19orf12):c.324C>T (p.Thr108=) rs10424582 0.72163
NM_031448.6(C19orf12):c.*1020C>A rs1140197 0.71321
NM_031448.6(C19orf12):c.*1114C>G rs1048123 0.44699
NM_031448.6(C19orf12):c.*1144C>T rs9566 0.41904
NM_001031726.3(C19orf12):c.*3819T>G rs11879584 0.16068
NM_031448.6(C19orf12):c.*1219C>T rs1129852 0.15013
NM_031448.6(C19orf12):c.*2100G>T rs74854677 0.09891
NM_031448.6(C19orf12):c.*3463G>A rs150123154 0.07814
NM_031448.6(C19orf12):c.*3336C>T rs10414583 0.05947
NM_031448.6(C19orf12):c.*1145G>A rs62105840 0.05157
NM_031448.6(C19orf12):c.*2662C>T rs78094750 0.04826
NM_031448.6(C19orf12):c.*2186C>T rs73548135 0.01436
NM_031448.6(C19orf12):c.*1666G>A rs116378078 0.01091
NM_031448.6(C19orf12):c.*3571C>T rs74868577 0.01087
NM_031448.6(C19orf12):c.*579C>T rs116245746 0.01082
NM_031448.6(C19orf12):c.*3372C>T rs117537955 0.01080
NM_031448.6(C19orf12):c.*47T>C rs111959875 0.01048
NM_031448.6(C19orf12):c.*2763A>G rs113735809 0.01028
NM_031448.6(C19orf12):c.-11+181T>C rs186970109 0.00552
NM_031448.6(C19orf12):c.392A>C (p.Lys131Thr) rs79915936 0.00444
NM_031448.6(C19orf12):c.*84C>T rs117867574 0.00423
NM_031448.6(C19orf12):c.*1170C>A rs75930446 0.00420
NM_031448.6(C19orf12):c.*2117G>A rs184117483 0.00302
NM_031448.6(C19orf12):c.*2778C>T rs80024917 0.00183
NM_031448.6(C19orf12):c.*2893G>A rs571030466 0.00163
NM_031448.6(C19orf12):c.*944A>G rs549030034 0.00002
NM_031448.6(C19orf12):c.*1361C>T rs189239161
NM_031448.6(C19orf12):c.*1362G>A rs113343769
NM_031448.6(C19orf12):c.*2790dup rs35730141
NM_031448.6(C19orf12):c.*3227_*3229del rs60814860
NM_031448.6(C19orf12):c.*3518C>A rs62105838
NM_031448.6(C19orf12):c.*437C>G rs1048104

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