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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL1RN
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
+5 more
GBenign/Likely benign
IL1RN
(I37T +3 more)
Single nucleotide variant
(missense variant)
Sterile multifocal osteomyelitis with periostitis and pustulosis
+2 more
GUncertain significance
IL1RN
Single nucleotide variant
(synonymous variant)
Sterile multifocal osteomyelitis with periostitis and pustulosis
+2 more
GLikely benign
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