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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NHS
(R247C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GLikely benign
NHS
(F756S +3 more)
Single nucleotide variant
(missense variant)
Nance-Horan syndrome
+2 more
GBenign/Likely benign
NHS
(M690T +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
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