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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLCO2A1
(R603*)
Single nucleotide variant
(nonsense)
Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
+1 more
GPathogenic/Likely pathogenic
SLCO2A1
Deletion
(inframe_deletion)
Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
GLikely pathogenic
SLCO2A1
Single nucleotide variant
(splice donor variant)
Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
+1 more
GPathogenic
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