Variant (rsID / SNP)
rs2350629
rs2350629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM118A. Location: chromosome 22, position 45,731,050. The table records no clinical significance for this variant.
Reference-table entries
FAM118ANot classified
- Variant type
- intron_variant
- Chromosome / position
- 22:45731050
- HGVS
- NM_001349916.2,c.980-181A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.