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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INSR
(V932L +1 more)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
INSR
(G749S)
Single nucleotide variant
(intron variant +1 more)
Rabson-Mendenhall syndrome
+3 more
GUncertain significance