Variant (rsID / SNP)
rs1105168
rs1105168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT2. Location: chromosome 5, position 150,886,882. The table records no clinical significance for this variant.
Reference-table entries
FAT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:150886882
- HGVS
- NM_001447.3,c.12350C>T,p.Pro4117Leu
- Allele change
- Missense_P4117L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.