Variant (rsID / SNP)
rs35025963
rs35025963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN3. Location: chromosome 19, position 8,191,184. The table records no clinical significance for this variant.
Reference-table entries
FBN3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:8191184
- HGVS
- NM_001321431.2,c.2602G>A,p.Asp868Asn
- Allele change
- Missense_D868N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.