Variant (rsID / SNP)
rs1565073
rs1565073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK10. Location: chromosome 2, position 225,634,693. The table records no clinical significance for this variant.
Reference-table entries
DOCK10Not classified
- Variant type
- intron_variant
- Chromosome / position
- 2:225634693
- HGVS
- NM_001363762.1,c.6483+235A>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
