List of variants reported as benign for Primary hypomagnesemia

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_006580.4(CLDN16):c.*1763T>A	rs9844654	0.84514
NM_006580.4(CLDN16):c.*794T>C	rs2293532	0.19740
NM_006580.4(CLDN16):c.114+10T>C	rs1491994	0.18734
NM_006580.4(CLDN16):c.-45G>C	rs3214506	0.18663
NM_006580.4(CLDN16):c.*1117G>A	rs10470534	0.17644
NM_006580.4(CLDN16):c.*842C>T	rs77656241	0.09613
NM_006580.4(CLDN16):c.*907A>G	rs116488781	0.02277
NM_006580.4(CLDN16):c.*1833G>A	rs116119310	0.02172
NM_006580.4(CLDN16):c.*1779A>C	rs115514339	0.01992
NM_006580.4(CLDN16):c.*204C>T	rs73053979	0.01330
NM_006580.4(CLDN16):c.*1453G>C	rs13076274	0.01276
NM_006580.4(CLDN16):c.620A>G (p.Tyr207Cys)	rs35041121	0.00671
NM_006580.4(CLDN16):c.*1234A>C	rs144651280	0.00638
NM_006580.4(CLDN16):c.*243C>T	rs142380851	0.00278
NM_006580.4(CLDN16):c.*2098T>G	rs187708101	0.00276
NM_006580.4(CLDN16):c.45C>G (p.Phe15Leu)	rs149116671	0.00248
NM_006580.4(CLDN16):c.532T>C (p.Leu178=)	rs143316426	0.00135
NM_006580.4(CLDN16):c.-45del	rs368234054

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