Variant (rsID / SNP)
rs2230365
rs2230365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFKBIL1. Location: chromosome 6, position 31,525,448. The table records no clinical significance for this variant.
Reference-table entries
NFKBIL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31525448
- HGVS
- NM_005007.4,c.378C>T,p.Ser126Ser
- Allele change
- Synonymous_S103S
Associated conditions / phenotypes
Autism Spectrum Disorder|Tic Disorder|Autoimmune Disease|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.