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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IGF2, INS-IGF2
(C71R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
INS, INS-IGF2
Single nucleotide variant
(intron variant)
not provided
+3 more
GPathogenic/Likely risk allele