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Links from MedGen

Items: 88

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF9
(W144R)
Single nucleotide variant
(missense variant)
Multiple synostoses syndrome 3
GLikely pathogenic
FGF9
(L4S)
Single nucleotide variant
(missense variant)
Multiple synostoses syndrome 3
GLikely pathogenic
FGF9
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
(R62G)
Single nucleotide variant
(missense variant)
Multiple synostoses syndrome 3
GPathogenic
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
FGF9
Single nucleotide variant
(synonymous variant)
Multiple synostoses syndrome 3
+1 more
GBenign
FGF9
Single nucleotide variant
(synonymous variant)
Multiple synostoses syndrome 3
+1 more
GBenign
FGF9
(L95V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FGF9
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GBenign
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
Single nucleotide variant
(5 prime UTR variant)
Multiple synostoses syndrome 3
GUncertain significance
FGF9
(S99N)
Single nucleotide variant
(missense variant)
Multiple synostoses syndrome 3
GPathogenic
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