ClinVar Miner

List of variants reported as benign for C3 glomerulonephritis

Included ClinVar conditions (1):
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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_030787.4(CFHR5):c.-20T>C rs9427662 0.19169
NM_030787.4(CFHR5):c.58+17T>A rs3748557 0.17992
NM_030787.4(CFHR5):c.434G>A (p.Gly145Glu) rs57960694 0.03706
NM_030787.4(CFHR5):c.507C>T (p.Asp169=) rs34533956 0.01500
NM_030787.4(CFHR5):c.254-8T>G rs114023763 0.01451
NM_030787.4(CFHR5):c.330A>C (p.Val110=) rs61745675 0.01447
NM_030787.4(CFHR5):c.832G>A (p.Gly278Ser) rs139017763 0.00815
NM_030787.4(CFHR5):c.1704T>A (p.Cys568Ter) rs143140599 0.00764
NM_030787.4(CFHR5):c.429T>C (p.Thr143=) rs140215003 0.00665
NM_030787.4(CFHR5):c.243G>A (p.Pro81=) rs7532068 0.00444
NM_030787.4(CFHR5):c.1586T>G (p.Leu529Arg) rs16840956 0.00386
NM_030787.4(CFHR5):c.732C>T (p.Asn244=) rs41306229 0.00250
NM_030787.4(CFHR5):c.1116C>T (p.Asn372=) rs556270179 0.00009
NM_030787.4(CFHR5):c.486dup (p.Glu163fs) rs565457964

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