Variant (rsID / SNP)
rs17876032
rs17876032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F12, SLC34A1. Location: chromosome 5, position 176,830,627. Clinical significance in the table: Benign.
Reference-table entries
F12Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:176830627
- Cytoband
- 5q35.3
- HGVS
- NM_000505.4(F12):c.1251-9C>T
- Allele change
- Silent
Associated conditions / phenotypes
Nephrolithiasis/osteoporosis, hypophosphatemic|Hereditary angioneurotic edema|Factor XII deficiency disease|Hereditary angioedema type 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.