Variant (rsID / SNP)
rs2271536
rs2271536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF19. Location: chromosome 17, position 72,351,406. The table records no clinical significance for this variant.
Reference-table entries
KIF19Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:72351406
- HGVS
- NM_153209.4,c.2952C>T,p.His984His
- Allele change
- Synonymous_H984H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
