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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059197, LOC130059198
+575 more
Copy number gain
See cases
GPathogenic
ACD, AGRP
+217 more
Copy number loss
See cases
GPathogenic
LCAT, SLC12A4
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GBenign
LCAT, SLC12A4
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GBenign
LCAT, SLC12A4
Single nucleotide variant
(3 prime UTR variant)
not provided
GLikely benign
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