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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935726, LOC129935727
+1665 more
Copy number gain
See cases
GPathogenic
LOC129935732, MFF
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
LOC129935732, MFF
Single nucleotide variant
(intron variant)
not provided
GBenign
LOC129935732, MFF
Deletion
(intron variant)
not provided
GBenign
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