Variant (rsID / SNP)
rs1488689
rs1488689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA22. Location: chromosome 17, position 3,352,294. The table records no clinical significance for this variant.
Reference-table entries
SPATA22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:3352294
- HGVS
- NM_001170695.2,c.479T>C,p.Ile160Thr
- Allele change
- Missense_I160T
Associated conditions / phenotypes
Missense_I160T|Missense_I117T|Missense_I160T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.