Variant (rsID / SNP)
rs61753162
rs61753162 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.436G>A (p.Glu146Lys)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.