List of variants reported as benign for Hereditary spherocytosis type 4

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000342.4(SLC4A1):c.*1568G>A	rs5033	0.63671
NM_000342.4(SLC4A1):c.*333C>A	rs2072081	0.36187
NM_000342.4(SLC4A1):c.*349G>A	rs1465204	0.05293
NM_000342.4(SLC4A1):c.1323G>A (p.Leu441=)	rs5017	0.05230
NM_000342.4(SLC4A1):c.166A>G (p.Lys56Glu)	rs5036	0.05002
NM_000342.4(SLC4A1):c.*270G>A	rs5027	0.04383
NM_000342.4(SLC4A1):c.1249C>T (p.Leu417=)	rs5015	0.03061
NM_000342.4(SLC4A1):c.2584G>A (p.Val862Ile)	rs5026	0.02980
NM_000342.4(SLC4A1):c.113A>C (p.Asp38Ala)	rs5035	0.02695
NM_000342.4(SLC4A1):c.*1721G>A	rs62078947	0.02193
NM_000342.4(SLC4A1):c.*897G>A	rs5030	0.02004
NM_000342.4(SLC4A1):c.2688T>C (p.Asp896=)	rs45497993	0.01896
NM_000342.4(SLC4A1):c.2712C>T (p.Tyr904=)	rs45519733	0.01857
NM_000342.4(SLC4A1):c.924G>A (p.Leu308=)	rs5013	0.01720
NM_000342.4(SLC4A1):c.*408C>T	rs45555735	0.01626
NM_000342.4(SLC4A1):c.1770G>A (p.Lys590=)	rs35807245	0.01536
NM_000342.4(SLC4A1):c.16-14G>A	rs145502796	0.01351
NM_000342.4(SLC4A1):c.1878T>C (p.Asp626=)	rs5020	0.01332
NM_000342.3(SLC4A1):c.118G>A (p.Glu40Lys)	rs45562031	0.01150
NM_000342.4(SLC4A1):c.2100C>T (p.Ser700=)	rs5024	0.01001
NM_000342.4(SLC4A1):c.1239C>T (p.Tyr413=)	rs5014	0.00887
NM_000342.4(SLC4A1):c.*335G>A	rs13306777	0.00773
NM_000342.4(SLC4A1):c.1953C>T (p.His651=)	rs5021	0.00529
NM_000342.4(SLC4A1):c.216G>T (p.Glu72Asp)	rs13306788	0.00342
NM_000342.4(SLC4A1):c.539G>A (p.Arg180His)	rs147390654	0.00294
NM_000342.4(SLC4A1):c.2561C>T (p.Pro854Leu)	rs2285644	0.00284
NM_000342.4(SLC4A1):c.1314G>A (p.Ser438=)	rs13306781	0.00193
NM_000342.4(SLC4A1):c.2716G>C (p.Glu906Gln)	rs199694087	0.00128
NM_000342.4(SLC4A1):c.*135G>A	rs566741511	0.00004

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