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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130060786, LOC130060787
+633 more
Copy number gain
See cases
GPathogenic
MED24
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
MED24
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
MED24
Single nucleotide variant
(intron variant)
not provided
GBenign
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