Variant (rsID / SNP)
rs4355234
rs4355234 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRTAP. Location: chromosome 3, position 33,186,087. Clinical significance in the table: Benign.
Reference-table entries
CRTAPBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:33186087
- Cytoband
- 3p22.3
- HGVS
- NM_006371.5(CRTAP):c.*2147A>G
- Allele change
- Silent
Associated conditions / phenotypes
Osteogenesis imperfecta type 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.