Variant (rsID / SNP)
rs114615136
rs114615136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLI3. Location: chromosome 7, position 42,003,187. Clinical significance in the table: Benign.
Reference-table entries
GLI3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:42003187
- Cytoband
- 7p14.1
- HGVS
- NM_000168.6(GLI3):c.*741A>G
- Allele change
- Silent
Associated conditions / phenotypes
Greig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.