List of variants in gene EPB41 reported as benign for hematologic disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001376013.1(EPB41):c.2314-19G>C	rs41266199	0.00973
NM_001376013.1(EPB41):c.1464-20T>C	rs139715164	0.00835
NM_001376013.1(EPB41):c.2019G>A (p.Lys673=)	rs79677225	0.00718
NM_001376013.1(EPB41):c.24G>A (p.Val8=)	rs75060926	0.00648
NM_001376013.1(EPB41):c.871C>T (p.Pro291Ser)	rs142874233	0.00467
NM_001376013.1(EPB41):c.120A>G (p.Gln40=)	rs146663694	0.00086
NM_001376013.1(EPB41):c.2577C>T (p.Thr859=)	rs536178

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