Variant (rsID / SNP)
rs1802029
rs1802029 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYROBP. Location: chromosome 19, position 36,395,446. Clinical significance in the table: Benign.
Reference-table entries
TYROBPBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:36395446
- Cytoband
- 19q13.12
- HGVS
- NM_003332.4(TYROBP):c.*25A>C
- Allele change
- Silent
Associated conditions / phenotypes
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.