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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC7A14
(F708V)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 68
GPathogenic
SLC7A14, SLC7A14-AS1
(C464F)
Single nucleotide variant
(missense variant)
SLC7A14-related condition
+2 more
GBenign/Likely benign
SLC7A14, SLC7A14-AS1
(G330R)
Single nucleotide variant
(missense variant)
SLC7A14-related condition
+3 more
GBenign/Likely benign
SLC7A14, SLC7A14-AS1
(A132V)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 68
GPathogenic
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