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

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004444.5(EPHB4):c.1752A>G (p.Gly584=)	rs314359	0.56302
NM_004444.5(EPHB4):c.1890C>T (p.Cys630=)	rs2230585	0.32365
NM_004444.5(EPHB4):c.1422+3A>G	rs3857809	0.08906
NM_004444.5(EPHB4):c.1314T>C (p.Ser438=)	rs144173

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