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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC105378448, LOC107195252
+245 more
Copy number loss
See cases
GPathogenic
LOC130004555, LOC130004556
+375 more
Copy number loss
See cases
GPathogenic
C10orf131, CC2D2B
+24 more
Copy number loss
See cases
GUncertain significance
ALDH18A1, LOC130004407
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
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