Variant (rsID / SNP)
rs11726117
rs11726117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK1. Location: chromosome 4, position 113,353,285. The table records no clinical significance for this variant.
Reference-table entries
ALPK1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:113353285
- HGVS
- NM_001102406.2,c.2582T>C,p.Met861Thr
- Allele change
- Missense_M783T
Associated conditions / phenotypes
Gout|Hyperuricemia|Paragangliomas 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.