Variant (rsID / SNP)
rs7605572
rs7605572 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFU1. Location: chromosome 2, position 69,646,504. Clinical significance in the table: Benign.
Reference-table entries
NFU1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:69646504
- Cytoband
- 2p13.3
- HGVS
- NM_001002755.4(NFU1):c.369+166C>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.