Variant (rsID / SNP)
rs724710
rs724710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCL2L11. Location: chromosome 2, position 111,907,691. The table records no clinical significance for this variant.
Reference-table entries
BCL2L11Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:111907691
- HGVS
- NM_138621.5,c.465T>C,p.Ile155Ile
- Allele change
- Silent
Associated conditions / phenotypes
Osteonecrosis|Childhood Acute Lymphocytic Leukemia|Leukemia, Acute Lymphoblastic|Myeloid Leukemia|Synonymous_I95I|Silent|Synonymous_I65I|Synonymous_I95I|Synonymous_I155I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.