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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCG, LOC101929532
(R21L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAP, LOC101929532
(L727P +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
FAP, LOC101929532
(Y720F +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
FAP, LOC101929532
(G735S +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
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