Variant (rsID / SNP)
rs2295524
rs2295524 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DGLUCY. Location: chromosome 14, position 91,671,124. The table records no clinical significance for this variant.
Reference-table entries
DGLUCYNot classified
- Variant type
- missense_variant
- Chromosome / position
- 14:91671124
- HGVS
- NM_001102368.3,c.1519G>A,p.Asp507Asn
- Allele change
- Missense_D502N
Associated conditions / phenotypes
Silent|Missense_D507N|Missense_D502N|Silent|Missense_D502N|Missense_D502N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.