Variant (rsID / SNP)
rs9603463
rs9603463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FREM2. Location: chromosome 13, position 39,455,266. Clinical significance in the table: Benign.
Reference-table entries
FREM2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:39455266
- Cytoband
- 13q13.3
- HGVS
- NM_207361.6(FREM2):c.*342G>A
- Allele change
- Silent
Associated conditions / phenotypes
Fraser syndrome 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.