Variant (rsID / SNP)
rs15786
rs15786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP13A2. Location: chromosome 1, position 17,312,592. Clinical significance in the table: Benign.
Reference-table entries
ATP13A2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:17312592
- Cytoband
- 1p36.13
- HGVS
- NM_022089.4(ATP13A2):c.*124C>T
- Allele change
- Silent
Associated conditions / phenotypes
Kufor-Rakeb syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.