Variant (rsID / SNP)
rs10951154
rs10951154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXA2, HOXA1. Location: chromosome 7, position 27,135,314. Clinical significance in the table: Benign.
Reference-table entries
HOXA2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:27135314
- Cytoband
- 7p15.2
- HGVS
- NM_005522.5(HOXA1):c.218G>A (p.Arg73His)
- Allele change
- Missense_R73H
Associated conditions / phenotypes
Bilateral microtia-deafness-cleft palate syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.