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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL1A2
(G358S)
Single nucleotide variant
(missense variant)
not provided
+9 more
GPathogenic
COL1A2
(G460S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta, perinatal lethal
+3 more
GPathogenic
COL1A2
(G550S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta with normal sclerae, dominant form
+2 more
GConflicting classifications of pathogenicity
COL1A2
(G601S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta, perinatal lethal
+5 more
GPathogenic
COL1A2
(G631V)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type III
+3 more
GPathogenic
COL1A2
(G772S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type I
+5 more
GPathogenic/Likely pathogenic
COL1A2
(C1195S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type III
+2 more
GPathogenic/Likely pathogenic
COL5A1
(P501fs)
Deletion
(frameshift variant)
Ehlers-Danlos syndrome, classic type, 1
+1 more
GPathogenic
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