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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDNRB, LOC107882129
(L55R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EDNRB, LOC107882129
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign/Likely benign
EDNRB, LOC107882129
(S4T)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
EDNRB, LOC107882129
(K3*)
Single nucleotide variant
(nonsense +1 more)
not specified
GUncertain significance
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