RRAS Chromosome 19
RAS related
Upload your DNA to see your personal genotypes for variants in RRAS.
What This Gene Does
The protein encoded by this gene is a small GTPase involved in diverse processes including angiogenesis, vascular homeostasis and regeneration, cell adhesion, and neuronal axon guidance. Mutations in this gene are found in many invasive cancers. [provided by RefSeq, Jul 2015]
Gene Info
Gene Group
RAS type GTPase family
Locus Type
gene with protein product
Location
19q13.33
Ensembl
ENSG00000126458
Associated Conditions (4)
Noonan syndrome
RRAS-related disorder
Malignant tumor of esophagus
Inborn genetic diseases
Key Variants
RS200611081
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS2230917
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS373359206
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS373517601
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS374621936
Conflicting classifications of pathogenicity
Noonan syndrome, RRAS-related disorder, Noonan syndrome
Health Risk
RS375821724
Conflicting classifications of pathogenicity
Noonan syndrome, RRAS-related disorder, Malignant tumor of esophagus
Health Risk
RS755223611
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS757080959
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS760978291
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS988964363
Conflicting classifications of pathogenicity
Noonan syndrome, Noonan syndrome
Health Risk
RS749539343
Likely pathogenic
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (11)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS200611081 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS2230917 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS373359206 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS373517601 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS374621936 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, RRAS-related disorder, Noonan syndrome |
| RS375821724 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, RRAS-related disorder, Malignant tumor of esophagus |
| RS755223611 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS757080959 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS760978291 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS988964363 | Health Risk | Conflicting classifications of pathogenicity | Noonan syndrome, Noonan syndrome |
| RS749539343 | Health Risk | Likely pathogenic | Inborn genetic diseases, Inborn genetic diseases |