Variant (rsID / SNP)
rs199533
rs199533 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NSF. Location: chromosome 17, position 44,828,931. The table records no clinical significance for this variant.
Reference-table entries
NSFNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:44828931
- HGVS
- NM_006178.4,c.2106G>A,p.Lys702Lys
- Allele change
- Synonymous_K702K
Associated conditions / phenotypes
Alzheimer Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.