Variant (rsID / SNP)
rs7406910
rs7406910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXB7. Location: chromosome 17, position 46,688,256. The table records no clinical significance for this variant.
Reference-table entries
HOXB7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:46688256
- HGVS
- NM_004502.4,c.25A>G,p.Thr9Ala
- Allele change
- Missense_T9A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.