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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861150, PLEKHA7
(V693I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
PLEKHA7
Single nucleotide variant
(synonymous variant)
PLEKHA7-related condition
+1 more
GBenign/Likely benign