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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALOX12B, ALOX15B
+141 more
Deletion
Li-Fraumeni syndrome
GPathogenic
LOC112533665, LOC116276454
+141 more
Deletion
Li-Fraumeni syndrome
+2 more
GPathogenic
TMEM107, LOC105371520
+1 more
(S73L +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC105371520, LOC130060224
+1 more
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
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