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Links from MedGen

Items: 19

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF862
(A938T)
Single nucleotide variant
(missense variant)
Gingival fibromatosis
GLikely pathogenic
SOS1
Single nucleotide variant
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Insertion
(3 prime UTR variant)
Noonan syndrome
+1 more
GLikely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Microsatellite
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome 4
+4 more
GBenign/Likely benign
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+4 more
GConflicting classifications of pathogenicity
SOS1
Duplication
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+1 more
GLikely benign
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+2 more
GConflicting classifications of pathogenicity
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Gingival fibromatosis
+4 more
GLikely benign
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+4 more
GLikely benign
SOS1
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GConflicting classifications of pathogenicity
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