Variant (rsID / SNP)
rs11858145
rs11858145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN1. Location: chromosome 15, position 33,359,574. The table records no clinical significance for this variant.
Reference-table entries
FMN1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 15:33359574
- HGVS
- NM_001103184.4,c.512G>T,p.Gly171Val
- Allele change
- Missense_G171V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.