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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAT2, LOC132089193
+1 more
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
FAT2, LOC132089193
+1 more
(R3518H)
Single nucleotide variant
(missense variant)
FAT2-related disorder
+1 more
GBenign/Likely benign
FAT2, LOC132089193
+1 more
(L3514S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
FAT2, LOC132089193
+1 more
Single nucleotide variant
(synonymous variant)
FAT2-related disorder
+1 more
GBenign
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