Variant (rsID / SNP)
rs509749
rs509749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LY9. Location: chromosome 1, position 160,793,560. The table records no clinical significance for this variant.
Reference-table entries
LY9Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:160793560
- HGVS
- NM_002348.4,c.1804A>G,p.Met602Val
- Allele change
- Missense_M602V
Associated conditions / phenotypes
Myeloma, Multiple|Systemic Lupus Erythematosus|Rheumatoid Arthritis|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.