Variant (rsID / SNP)
rs3825807
rs3825807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS7. Location: chromosome 15, position 79,089,111. Clinical significance in the table: Benign.
Reference-table entries
ADAMTS7Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 15:79089111
- HGVS
- NM_014272.5,c.640T>C,p.Ser214Pro
- Allele change
- Missense_S214P
Associated conditions / phenotypes
Vascular Disease|Peripheral Artery Disease|Peripheral Vascular Disease|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Rheumatoid Arthritis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.