List of variants in gene SLC4A1 reported as likely benign for Hereditary spherocytosis type 4

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000342.4(SLC4A1):c.166A>G (p.Lys56Glu)	rs5036	0.05002
NM_000342.3(SLC4A1):c.118G>A (p.Glu40Lys)	rs45562031	0.01150
NM_000342.4(SLC4A1):c.*1227A>C	rs141425539	0.00288
NM_000342.4(SLC4A1):c.-60G>A	rs75489266	0.00245
NM_000342.4(SLC4A1):c.*1792G>A	rs143785442	0.00184
NM_000342.4(SLC4A1):c.-135G>A	rs183529485	0.00173
NM_000342.4(SLC4A1):c.-30C>T	rs148028272	0.00167
NM_000342.4(SLC4A1):c.884G>A (p.Arg295His)	rs140424071	0.00065
NM_000342.4(SLC4A1):c.349+15C>G	rs541501285	0.00054
NM_000342.4(SLC4A1):c.*1237C>T	rs774513767	0.00048
NM_000342.4(SLC4A1):c.457C>A (p.Leu153Met)	rs145041032	0.00044
NM_000342.4(SLC4A1):c.*1933G>A	rs565128885	0.00034
NM_000342.4(SLC4A1):c.*947C>G	rs368389948	0.00029
NM_000342.4(SLC4A1):c.798T>C (p.Phe266=)	rs193011645	0.00023
NM_000342.4(SLC4A1):c.-136C>T	rs566359654	0.00016
NM_000342.4(SLC4A1):c.286C>T (p.Arg96Cys)	rs538778224
NM_000342.4(SLC4A1):c.92T>C (p.Met31Thr)	rs55773290

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