Variant (rsID / SNP)
rs3816527
rs3816527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTX3. Location: chromosome 3, position 157,155,314. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 3:157155314
- HGVS
- NM_002852.4,c.143C>A,p.Ala48Asp
- Allele change
- Silent
Associated conditions / phenotypes
Migraine with or Without Aura 1|Headache|Chronic Kidney Disease|Kidney Disease|Aspergillosis|Invasive Aspergillosis|Pulmonary Disease, Chronic Obstructive|Allergic Bronchopulmonary Aspergillosis|Cryptococcosis|Fungal Infectious Disease|Oral Cancer|Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis|Coronary Heart Disease 1|Pneumonia|Mycobacterium Tuberculosis 1|Cervical Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.