Variant (rsID / SNP)
rs1399078
rs1399078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN1. Location: chromosome 15, position 33,446,947. The table records no clinical significance for this variant.
Reference-table entries
FMN1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 15:33446947
- HGVS
- NM_001277313.2,c.169T>G,p.Ser57Ala
- Allele change
- Missense_S57A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.