Variant (rsID / SNP)
rs3750920
rs3750920 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOLLIP. Location: chromosome 11, position 1,309,956. The table records no clinical significance for this variant.
Reference-table entries
TOLLIPNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:1309956
- HGVS
- NM_019009.4,c.417G>A,p.Pro139Pro
- Allele change
- Synonymous_P89P
Associated conditions / phenotypes
Interstitial Lung Disease 2|Pulmonary Fibrosis|Lung Disease|Disease by Infectious Agent|Fibrosis of Extraocular Muscles, Congenital, 1|Plasmodium Vivax Malaria|Malaria|Lepromatous Leprosy|Leprosy 3|Kala-Azar 1|Leishmaniasis|Cutaneous Leishmaniasis|Allergic Disease|Mycobacterium Tuberculosis 1|Pneumonia|Extrinsic Allergic Alveolitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.