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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPGR
Single nucleotide variant
(stop lost +1 more)
Retinitis pigmentosa 3
GLikely pathogenic
RPGR
(R780fs)
Microsatellite
(frameshift variant +1 more)
Retinitis pigmentosa 3
GPathogenic
RPGR
(E746fs)
Microsatellite
(frameshift variant +1 more)
X-linked cone-rod dystrophy 1
+7 more
GPathogenic/Likely pathogenic
RPGR
Deletion
(intron variant)
Retinitis pigmentosa 3
GUncertain significance
RPGR
(A163T +2 more)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 3
GUncertain significance
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