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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIMIP2A, STPG3
+1 more
(L79P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CIMIP2A, STPG3
+1 more
(E150K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CIMIP2A, STPG3
+1 more
(D223H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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