Variant (rsID / SNP)
rs3762648
rs3762648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPPA4. Location: chromosome 3, position 109,052,732. The table records no clinical significance for this variant.
Reference-table entries
DPPA4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:109052732
- HGVS
- NM_018189.4,c.163A>G,p.Ile55Val
- Allele change
- Missense_I55V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.