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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPM1
(S1617fs +2 more)
Duplication
(frameshift variant)
Congenital stationary night blindness 1C
GPathogenic
ARHGAP11B, CHRFAM7A
+11 more
Copy number gain
Short attention span
+12 more
GPathogenic