List of variants in gene combination EPHB4, LOC126860124 reported as uncertain significance for immune system disorder

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004444.5(EPHB4):c.2522C>T (p.Pro841Leu)
NM_004444.5(EPHB4):c.2567G>A (p.Cys856Tyr)	rs1584653005
NM_004444.5(EPHB4):c.2576A>G (p.Lys859Arg)

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