Variant (rsID / SNP)
rs1050998
rs1050998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CXCL16. Location: chromosome 17, position 4,638,737. The table records no clinical significance for this variant.
Reference-table entries
CXCL16Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:4638737
- HGVS
- NM_001100812.2,c.368T>C,p.Ile123Thr
- Allele change
- Missense_I142T
Associated conditions / phenotypes
Myocardial Infarction
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.