Variant (rsID / SNP)
rs12314553
rs12314553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPY19L2. Location: chromosome 12, position 63,954,300. The table records no clinical significance for this variant.
Reference-table entries
DPY19L2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:63954300
- HGVS
- NM_173812.5,c.2269G>A,p.Val757Ile
- Allele change
- Missense_V757I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.