List of variants in gene EPHA2 reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004431.5(EPHA2):c.1896G>A (p.Leu632=)	rs55655135	0.00541
NM_004431.5(EPHA2):c.1314G>A (p.Glu438=)	rs55700006	0.00355
NM_004431.5(EPHA2):c.489G>A (p.Leu163=)	rs146626026	0.00153
NM_004431.5(EPHA2):c.2579G>A (p.Arg860His)	rs139225059	0.00049
NM_004431.5(EPHA2):c.1712C>T (p.Pro571Leu)	rs376402047	0.00012

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