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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EGF, LOC126807134
(P698A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EGF, LOC126807134
(Y747H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
EGF, LOC126807134
(G708R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EGF, LOC126807134
(D734G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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