Variant (rsID / SNP)
rs35697540
rs35697540 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAV1. Location: chromosome 7, position 116,165,160. Clinical significance in the table: Benign.
Reference-table entries
CAV1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:116165160
- Cytoband
- 7q31.2
- HGVS
- NM_001753.5(CAV1):c.30+14G>T
- Allele change
- Silent
Associated conditions / phenotypes
Pulmonary hypertension, primary, 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.