Variant (rsID / SNP)
rs870849
rs870849 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAG3. Location: chromosome 12, position 6,887,020. The table records no clinical significance for this variant.
Reference-table entries
LAG3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:6887020
- HGVS
- NM_002286.6,c.1364T>C,p.Ile455Thr
- Allele change
- Missense_I455T
Associated conditions / phenotypes
Autoimmune Disease|Thrombocytopenia Due to Platelet Alloimmunization|Thrombocytopenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.