Variant (rsID / SNP)
rs3844283
rs3844283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAK2. Location: chromosome 3, position 10,264,480. The table records no clinical significance for this variant.
Reference-table entries
IRAK2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:10264480
- HGVS
- NM_001570.4,c.1174C>G,p.Leu392Val
- Allele change
- Missense_L392V
Associated conditions / phenotypes
Systemic Lupus Erythematosus|Autoimmune Disease|Lupus Erythematosus|Rheumatoid Arthritis|Arthritis|Hepatitis C|Hepatitis C Virus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.