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Links from MedGen

Items: 89

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRAS
(I36M)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
GLikely pathogenic
NRAS
(G60V)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
+1 more
GConflicting classifications of pathogenicity
NRAS
(Q150R)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
GLikely pathogenic
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(intron variant)
RASopathy
+2 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
(V9I)
Single nucleotide variant
(missense variant)
RASopathy
+8 more
GUncertain significance
NRAS
(I84V)
Single nucleotide variant
(missense variant)
RASopathy
+2 more
GUncertain significance
NRAS
Single nucleotide variant
(synonymous variant)
NRAS-related disorder
+5 more
GBenign/Likely benign
LOC129931249, NRAS
Single nucleotide variant
(5 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
(T127R)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
+1 more
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
+1 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GBenign
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GUncertain significance
NRAS
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 6
GLikely benign
NRAS
(Q61P)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
NRAS
(S106L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
NRAS
(P185S)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
+3 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(synonymous variant)
Noonan syndrome 6
+5 more
GBenign/Likely benign
NRAS
(G12S)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
+3 more
GPathogenic
LOC129931249, NRAS
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GBenign/Likely benign
NRAS
Single nucleotide variant
(intron variant)
not provided
+5 more
GConflicting classifications of pathogenicity
NRAS
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
NRAS
(A59T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
NRAS
(G12R)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
+2 more
GPathogenic
NRAS
(G12D)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+6 more
GPathogenic/Likely pathogenic
NRAS
(G60E)
Single nucleotide variant
(missense variant)
NRAS-related disorder
+3 more
GPathogenic
NRAS
(T50I)
Single nucleotide variant
(missense variant)
RASopathy
+1 more
GPathogenic
NRAS
(G13D)
Single nucleotide variant
(missense variant)
Acute megakaryoblastic leukemia in down syndrome
+2 more
GPathogenic/Likely pathogenic
NRAS
(Q61R)
Single nucleotide variant
(missense variant)
Large congenital melanocytic nevus
+3 more
GConflicting classifications of pathogenicity
NRAS
(G13R)
Single nucleotide variant
(missense variant)
Noonan syndrome 6
GLikely pathogenic
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