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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFNAR2, IFNAR2-IL10RB
(R324H)
Single nucleotide variant
(missense variant +2 more)
Immunodeficiency 45
GUncertain significance
IFNAR2-IL10RB, IL10RB
(T72M)
Single nucleotide variant
(missense variant)
Inflammatory bowel disease 25
GConflicting classifications of pathogenicity
IFNAR2-IL10RB, IL10RB
(W100G)
Single nucleotide variant
(missense variant)
Inflammatory bowel disease 25
GUncertain significance
IFNAR2-IL10RB, IL10RB
Single nucleotide variant
(splice donor variant)
Inflammatory bowel disease 25
GLikely pathogenic
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