Variant (rsID / SNP)
rs1555839
rs1555839 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA, LIPJ. Location: chromosome 10, position 90,382,820. The table records no clinical significance for this variant.
Reference-table entries
NANot classified
- Variant type
- intergenic_region
- Chromosome / position
- 10:90382820
- HGVS
- NA,n.90382820C>T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.