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Links from MedGen

Items: 64

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSX2
(P148fs)
Duplication
(3 prime UTR variant +1 more)
Craniosynostosis 2
GPathogenic
MSX2
(A238T)
Single nucleotide variant
(3 prime UTR variant +1 more)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
(H265Y)
Single nucleotide variant
(3 prime UTR variant +1 more)
Craniosynostosis 2
GUncertain significance
MSX2
(S234fs)
Duplication
(3 prime UTR variant +1 more)
Craniosynostosis 2
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign/Likely benign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+2 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
(P251S)
Single nucleotide variant
(3 prime UTR variant +1 more)
Cranium bifidum occultum
+2 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
(K105N)
Single nucleotide variant
(missense variant)
Craniosynostosis 2
+1 more
GBenign/Likely benign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
(A102T)
Single nucleotide variant
(missense variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
(V96L)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MSX2
(K41M)
Single nucleotide variant
(missense variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(5 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GBenign
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
Parietal foramina 1
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MSX2
Single nucleotide variant
(3 prime UTR variant +1 more)
Cranium bifidum occultum
+2 more
GBenign
MSX2
(A212G)
Single nucleotide variant
(3 prime UTR variant +1 more)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
Single nucleotide variant
(5 prime UTR variant)
not provided
+2 more
GBenign
MSX2
Single nucleotide variant
(5 prime UTR variant)
Craniosynostosis 2
+1 more
GBenign/Likely benign
MSX2
Single nucleotide variant
(5 prime UTR variant)
Craniosynostosis 2
+1 more
GUncertain significance
MSX2
(M129T)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+4 more
GBenign
MSX2
(P148L)
Single nucleotide variant
(missense variant +1 more)
Cranium bifidum occultum
GPathogenic
MSX2
(P148H)
Single nucleotide variant
(3 prime UTR variant +1 more)
Cranium bifidum occultum
GPathogenic
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