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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DISC2, DISC1
+1 more
(D484H +3 more)
Single nucleotide variant
(non-coding transcript variant +3 more)
Inborn genetic diseases
GUncertain significance
DISC2, DISC1
+1 more
(S504N +2 more)
Single nucleotide variant
(non-coding transcript variant +3 more)
Inborn genetic diseases
GLikely benign
TSNAX-DISC1, DISC2
+1 more
(L649P +2 more)
Single nucleotide variant
(non-coding transcript variant +3 more)
Inborn genetic diseases
GUncertain significance
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