Variant (rsID / SNP)
rs6650971
rs6650971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT2. Location: chromosome 5, position 150,901,261. The table records no clinical significance for this variant.
Reference-table entries
FAT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:150901261
- HGVS
- NM_001447.3,c.10893G>A,p.Met3631Ile
- Allele change
- Missense_M3631I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.