Variant (rsID / SNP)
rs11073001
rs11073001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL16. Location: chromosome 15, position 81,592,802. The table records no clinical significance for this variant.
Reference-table entries
IL16Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:81592802
- HGVS
- NM_001352686.2,c.3288A>G,p.Thr1096Thr
- Allele change
- Synonymous_T435T
Associated conditions / phenotypes
Autoimmune Disease|Alopecia Areata|Alopecia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.