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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RP9
Deletion
(frameshift variant +1 more)
Retinitis Pigmentosa, Dominant
+3 more
GBenign/Likely benign
RP9
(K210R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
RP9
(V155I)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
RP9
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
RP9
(G97E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RP9
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
LOC129998225, RP9
(A12T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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