List of variants in gene EPB42 reported as benign for hereditary spherocytosis

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001114134.2(EPB42):c.833-4A>G	rs61343376	0.05117
NM_001114134.2(EPB42):c.-51T>C	rs16957499	0.05107
NM_001114134.2(EPB42):c.330G>A (p.Ala110=)	rs1042168	0.03903
NM_001114134.2(EPB42):c.10+19C>T	rs77809780	0.02853
NM_001114134.2(EPB42):c.654+7G>A	rs72721553	0.01821
NM_001114134.2(EPB42):c.1318+4C>T	rs45498491	0.01529

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