Variant (rsID / SNP)
rs6798252
rs6798252 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF10. Location: chromosome 3, position 151,166,422. The table records no clinical significance for this variant.
Reference-table entries
IGSF10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:151166422
- HGVS
- NM_001385060.1,c.1347G>A,p.Gln449Gln
- Allele change
- Synonymous_Q449Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.