Variant (rsID / SNP)
rs150267769
rs150267769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPP7. Location: chromosome 9, position 140,008,443. The table records no clinical significance for this variant.
Reference-table entries
DPP7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 9:140008443
- HGVS
- NM_013379.3,c.359C>T,p.Ser120Phe
- Allele change
- Missense_S120F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.