List of variants reported as likely benign for chronic kidney disease

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val)	rs146496725	0.00537
NM_000091.5(COL4A3):c.346C>A (p.Pro116Thr)	rs115324397	0.00485
NM_000204.5(CFI):c.782G>A (p.Gly261Asp)	rs112534524	0.00153
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys)	rs201445955	0.00036

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