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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111A
(A188G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
FAM111A
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
FAM111A
(I433M)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
FAM111A
(C485Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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