ClinVar for MedGen (Select 326760) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 441023	NM_002116.8(HLA-A):c.776del (p.Pro259fs)	HLA-A (P259fs)	Deletion (frameshift variant)	Susceptibility to severe cutaneous adverse reaction	Gnot provided
Select item 14911	HLA–B*58:01	HLA-B	Variation	Stevens-Johnson syndrome, susceptibility to +2 more	Grisk factor
Select item 14909	HLA-B*15:02	HLA-B	Variation	Toxic epidermal necrolysis +2 more	Grisk factor

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