Variant (rsID / SNP)
rs16855642
rs16855642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LHX4. Location: chromosome 1, position 180,235,728. Clinical significance in the table: Benign.
Reference-table entries
LHX4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:180235728
- Cytoband
- 1q25.2
- HGVS
- NM_033343.4(LHX4):c.450C>T (p.Asn150=)
- Allele change
- Synonymous_N150N
Associated conditions / phenotypes
Short stature-pituitary and cerebellar defects-small sella turcica syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.