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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PAX2
(V26fs +1 more)
Duplication
(frameshift variant)
Renal coloboma syndrome
+2 more
GPathogenic
PAX2
(V26fs +1 more)
Deletion
(frameshift variant)
PAX2-related disorder
+2 more
GPathogenic
PAX2
(V42A +1 more)
Single nucleotide variant
(missense variant)
Renal coloboma syndrome
GUncertain significance
PAX2
(R59W +1 more)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 7
GLikely pathogenic
PAX2
(R102G +1 more)
Single nucleotide variant
(missense variant)
Renal coloboma syndrome
GUncertain significance
PAX2
(R137* +1 more)
Single nucleotide variant
(nonsense)
Renal coloboma syndrome
GPathogenic
PAX2
(G192R +1 more)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 7
GUncertain significance
PAX2
(R229* +2 more)
Single nucleotide variant
(nonsense)
Renal coloboma syndrome
+2 more
GPathogenic
PAX2
(Q264fs +2 more)
Deletion
(frameshift variant)
Renal coloboma syndrome
+1 more
GLikely pathogenic
PAX2
(K281fs +2 more)
Microsatellite
(frameshift variant)
Renal coloboma syndrome
GLikely pathogenic
PAX2
(P290fs +2 more)
Deletion
(frameshift variant)
Focal segmental glomerulosclerosis 7
GLikely pathogenic
PAX2
(E291* +2 more)
Single nucleotide variant
(nonsense)
Renal coloboma syndrome
GLikely pathogenic
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