Variant (rsID / SNP)
rs1248634
rs1248634 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLG5. Location: chromosome 10, position 79,579,222. The table records no clinical significance for this variant.
Reference-table entries
DLG5Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 10:79579222
- HGVS
- NM_004747.4,c.3528C>T,p.Gly1176Gly
- Allele change
- Synonymous_G1176G
Associated conditions / phenotypes
Inflammatory Bowel Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.