Variant (rsID / SNP)
rs56017170
rs56017170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLGAP1. Location: chromosome 18, position 3,581,966. The table records no clinical significance for this variant.
Reference-table entries
DLGAP1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:3581966
- HGVS
- NM_001398525.1,c.1902C>T,p.Thr634Thr
- Allele change
- Synonymous_T624T
Associated conditions / phenotypes
Synonymous_T322T|Synonymous_T340T|Synonymous_T624T|Synonymous_T322T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.