Variant (rsID / SNP)
rs5771069
rs5771069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17REL. Location: chromosome 22, position 50,435,480. The table records no clinical significance for this variant.
Reference-table entries
IL17RELNot classified
- Variant type
- missense_variant
- Chromosome / position
- 22:50435480
- HGVS
- NM_001001694.3,c.998T>C,p.Leu333Pro
- Allele change
- Missense_L333P
Associated conditions / phenotypes
Colitis|Ulcerative Colitis|Inflammatory Bowel Disease 17|Inflammatory Bowel Disease 11|Inflammatory Bowel Disease 1|Inflammatory Bowel Disease 23|Inflammatory Bowel Disease 7|Inflammatory Bowel Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.