List of variants in gene EFNB1 reported as likely pathogenic by Department of Medical Genetics, Oslo University Hospital

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004429.5(EFNB1):c.128+5G>A	rs2080439797
NM_004429.5(EFNB1):c.161C>T (p.Pro54Leu)	rs104894801
NM_004429.5(EFNB1):c.182A>G (p.Asp61Gly)	rs2080468583
NM_004429.5(EFNB1):c.635_636del (p.Val212fs)	rs2080473382

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