Related gene-specific medical variations for Gene (Select 3106) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3362234	NM_005514.8(HLA-B):c.620-3C>G	HLA-B	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 3362233	NM_005514.8(HLA-B):c.896-1G>A	HLA-B	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	Gnot provided
Select item 3342262	NM_005514.8(HLA-B):c.896-1G>C	HLA-B, MIR6891	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	Gnot provided
Select item 14911	HLA–B*58:01	HLA-B	Variation	Stevens-Johnson syndrome, susceptibility to +2 more	Grisk factor
Select item 14910	HLA-B*57:01	HCP5, HLA-B	Single nucleotide variant (non-coding transcript variant)	Drug-induced liver injury due to flucloxacillin +2 more	GPathogenic/Likely risk allele; risk factor
Select item 14909	HLA-B*15:02	HLA-B	Variation	Stevens-Johnson syndrome, susceptibility to +2 more	Grisk factor
Select item 14908	HLA-B*27	HLA-B	Variation	Synovitis, chronic, susceptibility to +1 more	Grisk factor

ClinVar