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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ETV6, LOC126861452
(L349P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely pathogenic
ETV6
Microsatellite
(intron variant)
See cases
+1 more
GPathogenic