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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM161A, LOC129933843
(G59E)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
FAM161A, LOC129933843
Single nucleotide variant
(synonymous variant +1 more)
Retinitis pigmentosa 28
+3 more
GBenign