Variant (rsID / SNP)
rs12925933
rs12925933 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM7. Location: chromosome 16, position 90,141,355. The table records no clinical significance for this variant.
Reference-table entries
PRDM7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:90141355
- HGVS
- NM_001098173.2,c.270T>G,p.Asp90Glu
- Allele change
- Missense_D90E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.