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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATM
(G204V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+1 more
GLikely benign