ClinVar Miner

List of variants in gene CYBB reported as benign for not provided

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000397.4(CYBB):c.141+90C>A rs4422908 0.32673
NM_000397.4(CYBB):c.484-1068T>C rs12014060 0.21793
NM_000397.4(CYBB):c.804+118A>G rs5964125 0.16667
NM_000397.4(CYBB):c.483+78C>T rs6610669 0.16506
NM_000397.4(CYBB):c.142-338G>T rs4595265 0.11896
NM_000397.4(CYBB):c.1002G>A (p.Lys334=) rs2228117 0.05579
NM_000397.4(CYBB):c.483+204T>C rs17146242 0.05290
NM_000397.4(CYBB):c.141+48C>G rs7059081 0.05245
NM_000397.4(CYBB):c.674+261A>C rs35959988 0.04423
NM_000397.4(CYBB):c.675-316T>A rs34052166 0.04407
NM_000397.4(CYBB):c.484-258C>T rs35851882 0.04211
NM_000397.4(CYBB):c.338-304A>G rs34097325 0.03518
NM_000397.4(CYBB):c.484-61A>G rs112709054 0.00189
NM_000397.4(CYBB):c.1414G>A (p.Gly472Ser) rs13306300 0.00018
NM_000397.4(CYBB):c.1314+19C>T rs34834015
NM_000397.4(CYBB):c.484-60TG[19] rs57325016
NM_000397.4(CYBB):c.484-60TG[20] rs57325016
NM_000397.4(CYBB):c.484-60TG[21] rs57325016
NM_000397.4(CYBB):c.484-60TG[24] rs57325016
NM_000397.4(CYBB):c.484-60TG[25] rs57325016
NM_000397.4(CYBB):c.897+239TG[20] rs58302662
NM_000397.4(CYBB):c.897+239TG[22] rs58302662
NM_000397.4(CYBB):c.897+239TG[23] rs58302662
NM_000397.4(CYBB):c.897+239TG[24] rs58302662
NM_000397.4(CYBB):c.897+239TG[25] rs58302662

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