List of variants in gene EPB41L2 reported as benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001431.4(EPB41L2):c.2550C>T (p.Asn850=)	rs141483573	0.00877
NM_001431.4(EPB41L2):c.1664C>T (p.Pro555Leu)	rs76682195	0.00809
NM_001431.4(EPB41L2):c.493-11_493-10del	rs34763200

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