List of variants in gene EPB41L1 reported as likely benign for Intellectual disability

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_012156.2(EPB41L1):c.1325T>A (p.Val442Asp)	rs1242238241	0.00001
NM_012156.2(EPB41L1):c.1600C>T (p.Arg534Trp)	rs375772370
NM_012156.2(EPB41L1):c.2269_2271del	rs2063600623

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