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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ENG, LOC102723566
(T203fs +1 more)
Deletion
(frameshift variant)
Telangiectasia, hereditary hemorrhagic, type 1
GLikely pathogenic
ENG
(R171*)
Single nucleotide variant
(nonsense +1 more)
Telangiectasia, hereditary hemorrhagic, type 1
+3 more
GPathogenic
ENG
(Y44H)
Single nucleotide variant
(missense variant +1 more)
Telangiectasia, hereditary hemorrhagic, type 1
+1 more
GUncertain significance
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