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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IAPP, SLCO1A2
(L13F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IAPP, SLCO1A2
(T23I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance