Variant (rsID / SNP)
rs8002697
rs8002697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LNX2. Location: chromosome 13, position 28,143,229. The table records no clinical significance for this variant.
Reference-table entries
LNX2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:28143229
- HGVS
- NM_153371.4,c.592T>C,p.Ser198Pro
- Allele change
- Missense_S198P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.