Variant (rsID / SNP)
rs2305913
rs2305913 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBF1. Location: chromosome 17, position 73,922,941. The table records no clinical significance for this variant.
Reference-table entries
FBF1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:73922941
- HGVS
- NM_001319193.2,c.493A>G,p.Arg165Gly
- Allele change
- Missense_R165G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.