List of variants in gene EPHB4 reported as likely benign for immune system disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004444.5(EPHB4):c.1743T>C (p.Tyr581=)	rs116240595	0.00915
NM_004444.5(EPHB4):c.1112C>T (p.Ala371Val)	rs55720981	0.00059

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