List of variants reported as benign for Familial hypokalemia-hypomagnesemia by Illumina Laboratory Services, Illumina

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.*205A>G	rs5805	0.63172
NM_001126108.2(SLC12A3):c.*664G>C	rs5808	0.62518
NM_001126108.2(SLC12A3):c.*931C>T	rs37030	0.60253
NM_001126108.2(SLC12A3):c.*1851A>G	rs37029	0.60231
NM_001126108.2(SLC12A3):c.*404C>T	rs37031	0.58188
NM_001126108.2(SLC12A3):c.*1524C>T	rs3812964	0.57598
NM_001126108.2(SLC12A3):c.*516T>A	rs11861555	0.49704
NM_001126108.2(SLC12A3):c.1670-8T>C	rs2304483	0.48985
NM_001126108.2(SLC12A3):c.2924+13C>T	rs2289115	0.34518
NM_001126108.2(SLC12A3):c.*1301A>C	rs9927820	0.29170
NM_001126108.2(SLC12A3):c.2721-13T>C	rs34772420	0.18153
NM_001126108.2(SLC12A3):c.1395C>T (p.Thr465=)	rs5801	0.15318
NM_001126108.2(SLC12A3):c.2142C>T (p.Ala714=)	rs5803	0.11388
NM_001126108.2(SLC12A3):c.2179-8C>T	rs13306676	0.11191
NM_001126108.2(SLC12A3):c.*975A>G	rs56079121	0.11158
NM_001126108.2(SLC12A3):c.*1674C>T	rs3812963	0.09905
NM_001126108.2(SLC12A3):c.2598C>T (p.Gly866=)	rs5804	0.09125
NM_001126108.2(SLC12A3):c.2711G>A (p.Arg904Gln)	rs11643718	0.08381
NM_001126108.2(SLC12A3):c.1884G>A (p.Ser628=)	rs5802	0.08069
NM_001126108.2(SLC12A3):c.366A>G (p.Ala122=)	rs2304479	0.05592
NM_001126108.2(SLC12A3):c.1023C>T (p.Phe341=)	rs2229209	0.04172
NM_001126108.2(SLC12A3):c.1825+9C>A	rs35797045	0.03711
NM_001126108.2(SLC12A3):c.2755C>T (p.Arg919Cys)	rs12708965	0.03475
NM_001126108.2(SLC12A3):c.*1204T>C	rs116537640	0.02034
NM_001126108.2(SLC12A3):c.*2432T>C	rs115344087	0.02023
NM_001126108.2(SLC12A3):c.1865A>G (p.Asn622Ser)	rs61746763	0.01422
NM_001126108.2(SLC12A3):c.*2068C>G	rs142540870	0.01329
NM_001126108.2(SLC12A3):c.3024C>T (p.Ile1008=)	rs2289113	0.01151
NM_001126108.2(SLC12A3):c.2964G>A (p.Ser988=)	rs35082264	0.00802
NM_001126108.2(SLC12A3):c.1539C>T (p.Tyr513=)	rs146805986	0.00597
NM_001126108.2(SLC12A3):c.1176C>T (p.Thr392=)	rs117440321

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