Variant (rsID / SNP)
rs61753168
rs61753168 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.501G>C (p.Lys167Asn)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.