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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKN2A
(G38V +1 more)
Single nucleotide variant
(missense variant +2 more)
Melanoma and neural system tumor syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(genic upstream transcript variant +1 more)
Melanoma-pancreatic cancer syndrome
+7 more
GPathogenic