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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHO
(I217S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RHO
(E247K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RHO
(D331H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RHO
(D331N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
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