Gene entry
RIT1
Ras like without CAAX 1
- Chromosome
- 1
- Cytoband
- 1q22
- Variants (rsID)
- 13
RIT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q22). Its official name is “Ras like without CAAX 1”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs1749409Benignsingle nucleotide variantNoonan syndrome 8
- rs483352822Pathogenicsingle nucleotide variantNoonan syndrome 8|Noonan syndrome|Noonan syndrome and Noonan-related syndrome|RASopathy
- rs672601334Pathogenicsingle nucleotide variantNoonan syndrome 8|Noonan syndrome|Noonan syndrome 1|Noonan syndrome and Noonan-related syndrome|RASopathy
- rs672601335Pathogenicsingle nucleotide variantNoonan syndrome 8|Noonan syndrome|RASopathy|Noonan syndrome and Noonan-related syndrome
- rs869025189Pathogenicsingle nucleotide variantNoonan syndrome|Noonan syndrome 8
- rs869025191Pathogenicsingle nucleotide variantNoonan syndrome|Noonan syndrome 8|Noonan syndrome 1
- rs869025193Pathogenicsingle nucleotide variantNoonan syndrome 8|Noonan syndrome|RASopathy|Inborn genetic diseases|Noonan syndrome and Noonan-related syndrome
- rs869025194Pathogenicsingle nucleotide variantNoonan syndrome 8|Noonan syndrome|RASopathy|Noonan syndrome and Noonan-related syndrome
- rs869025195Pathogenicsingle nucleotide variantNoonan syndrome|Inborn genetic diseases|Noonan syndrome 1|RASopathy|Noonan syndrome 8
- rs869025197Pathogenicsingle nucleotide variantNoonan syndrome|Noonan syndrome 8|Noonan syndrome and Noonan-related syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.