Variant (rsID / SNP)
rs522496
rs522496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF17. Location: chromosome 1, position 21,024,901. The table records no clinical significance for this variant.
Reference-table entries
KIF17Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:21024901
- HGVS
- NM_020816.4,c.1204G>A,p.Val402Met
- Allele change
- Missense_V302M
Associated conditions / phenotypes
Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.