Variant (rsID / SNP)
rs61758211
rs61758211 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAS. Location: chromosome 1, position 115,259,311. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
NRASBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:115259311
- Cytoband
- 1p13.2
- HGVS
- NM_002524.5(NRAS):c.-50A>G
- Allele change
- Silent
Associated conditions / phenotypes
Noonan syndrome 6
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.