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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GBenign/Likely benign
STK11
Microsatellite
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity