Variant (rsID / SNP)
rs1368464
rs1368464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRAS. Location: chromosome 19, position 50,140,068. Clinical significance in the table: Benign.
Reference-table entries
RRASBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:50140068
- Cytoband
- 19q13.33
- HGVS
- NM_006270.5(RRAS):c.344+13G>A
- Allele change
- Silent
Associated conditions / phenotypes
Noonan syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.