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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130062899, STK11
(V338M)
Single nucleotide variant
(missense variant)
Carcinoma of pancreas
+6 more
GConflicting classifications of pathogenicity
LOC130062899, STK11
(F354L)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+7 more
GBenign/Likely benign