Variant (rsID / SNP)
rs61752149
rs61752149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RS1. The table records no clinical significance for this variant.
Reference-table entries
RS1Not classified
- Variant type
- single nucleotide variant
- Cytoband
- Xp22.13
- HGVS
- NM_000330.4(RS1):c.380T>C (p.Leu127Pro)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.