Variant (rsID / SNP)
rs7535144
rs7535144 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLAD1, LENEP. Location: chromosome 1, position 154,965,113. Clinical significance in the table: Benign.
Reference-table entries
FLAD1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:154965113
- Cytoband
- 1q21.3
- HGVS
- NM_025207.5(FLAD1):c.1555-76G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.