Variant (rsID / SNP)
rs34237418
rs34237418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRAS1. Location: chromosome 4, position 78,979,141. Clinical significance in the table: Benign.
Reference-table entries
FRAS1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:78979141
- Cytoband
- 4q21.21
- HGVS
- NM_025074.7(FRAS1):c.-23C>T
- Allele change
- Silent
Associated conditions / phenotypes
Fraser syndrome 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.