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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACP2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ACP2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ACP2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ACP2
(G89D +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
NR1H3, ACP2
+1 more
(R29Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
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