Variant (rsID / SNP)
rs55716643
rs55716643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACP4. Location: chromosome 19, position 51,297,825. The table records no clinical significance for this variant.
Reference-table entries
ACP4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:51297825
- HGVS
- NM_033068.3,c.973G>A,p.Ala325Thr
- Allele change
- Missense_A325T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.