Variant (rsID / SNP)
rs328418
rs328418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT1. Location: chromosome 4, position 187,557,893. The table records no clinical significance for this variant.
Reference-table entries
FAT1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:187557893
- HGVS
- NM_005245.4,c.3818A>G,p.His1273Arg
- Allele change
- Missense_H1273R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
