List of variants in gene EPHB4 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_004444.5(EPHB4):c.1144G>A (p.Gly382Ser)	rs114926839	0.00239
NM_004444.5(EPHB4):c.691C>T (p.Pro231Ser)	rs147563837	0.00077
NM_004444.5(EPHB4):c.1692-6C>A	rs202035530	0.00052
NM_004444.5(EPHB4):c.918C>T (p.Val306=)	rs151161414	0.00036

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