List of variants in gene EPHA2 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004431.5(EPHA2):c.1941G>T (p.Thr647=)	rs56043737	0.01185
NM_004431.5(EPHA2):c.1486G>A (p.Asp496Asn)	rs115171763	0.00292
NM_004431.5(EPHA2):c.944G>A (p.Arg315Gln)	rs139176878	0.00147
NM_004431.5(EPHA2):c.2239G>A (p.Val747Ile)	rs145592908	0.00139
NM_004431.5(EPHA2):c.1407C>T (p.Tyr469=)	rs201532782	0.00083
NM_004431.5(EPHA2):c.2875G>A (p.Ala959Thr)	rs139787163	0.00036
NM_004431.5(EPHA2):c.121C>G (p.Leu41Val)	rs147977279	0.00023

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