Variant (rsID / SNP)
rs1141168
rs1141168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAK4. Location: chromosome 12, position 44,182,706. Clinical significance in the table: Benign.
Reference-table entries
IRAK4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:44182706
- Cytoband
- 12q12
- HGVS
- NM_016123.4(IRAK4):c.*2188A>G
- Allele change
- Silent
Associated conditions / phenotypes
Immunodeficiency 67
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.