Variant (rsID / SNP)
rs33998096
rs33998096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LHX3. Location: chromosome 9, position 139,092,571. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
LHX3Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:139092571
- Cytoband
- 9q34.3
- HGVS
- NM_178138.6(LHX3):c.108G>A (p.Gln36=)
- Allele change
- Synonymous_Q25Q
Associated conditions / phenotypes
Non-acquired combined pituitary hormone deficiency with spine abnormalities
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.