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Items: 1 to 100 of 773

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RRAS
(E88fs)
Deletion
(frameshift variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GUncertain significance
RRAS
(N178T)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(A85T)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(G10R)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(F123I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Deletion
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(Y97H)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
RRAS-related disorder
+1 more
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(A92T)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(T61N)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
LZTR1
(F666V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
+1 more
GLikely benign
RRAS
(V107M)
Single nucleotide variant
(missense variant)
Noonan syndrome
+1 more
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GUncertain significance
RRAS
(G17V)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(R113W)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(A5T)
Indel
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Deletion
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(C70Y)
Single nucleotide variant
(missense variant)
Noonan syndrome
+1 more
GUncertain significance
RRAS
(H165D)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(M1L)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(C215R)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(R191W)
Single nucleotide variant
(missense variant)
Noonan syndrome
+1 more
GUncertain significance
RRAS
(E28D)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(P200L)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(E181K)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(S204G)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(R15P)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(M98V)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(R15Q)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(L146M)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
+1 more
GLikely benign
RRAS
(M1V)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GUncertain significance
RRAS
Duplication
(intron variant)
Noonan syndrome
GBenign
RRAS
(R99C)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
RRAS
(V152I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(R15W)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
LZTR1
Single nucleotide variant
(splice acceptor variant)
Noonan syndrome
+1 more
GPathogenic
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
+1 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
+1 more
GLikely benign
LZTR1
(A477G)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
+1 more
GConflicting classifications of pathogenicity
RRAS
(A162T)
Single nucleotide variant
(missense variant)
Noonan syndrome
+1 more
GUncertain significance
RRAS
(R132H)
Single nucleotide variant
(missense variant)
Noonan syndrome
+1 more
GUncertain significance
RRAS
(P26L)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(A159P)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
LOC129933535, SOS1
(Q2K)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
+1 more
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Deletion
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GLikely benign
RRAS
(R150P)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
RRAS-related disorder
+1 more
GConflicting classifications of pathogenicity
RRAS
(V179M)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
RRAS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
RRAS
(M1K)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome
GUncertain significance
RRAS
(P24S)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
(P26fs)
Duplication
(frameshift variant)
Noonan syndrome
GUncertain significance
RRAS
(G39C)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
RRAS
Single nucleotide variant
(intron variant)
Noonan syndrome
GUncertain significance
RRAS
(E181Q)
Single nucleotide variant
(missense variant)
Noonan syndrome
GUncertain significance
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