Variant (rsID / SNP)
rs2278370
rs2278370 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT2. Location: chromosome 5, position 150,930,186. The table records no clinical significance for this variant.
Reference-table entries
FAT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:150930186
- HGVS
- NM_001447.3,c.4543G>A,p.Gly1515Ser
- Allele change
- Missense_G1515S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.