ClinVar for MedGen (Select 1684882) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717003	NM_001039660.2(IL18BP):c.67G>A (p.Val23Ile)	IL18BP (V23I)	Single nucleotide variant (missense variant)	Hepatitis, fulminant viral, susceptibility to +1 more	GLikely benign
Select item 689420	NM_001039660.2(IL18BP):c.508-19_528del	IL18BP	Deletion (splice acceptor variant +1 more)	Hepatitis, fulminant viral, susceptibility to	Grisk factor