Variant (rsID / SNP)
rs7200543
rs7200543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDXDC1. Location: chromosome 16, position 15,129,970. The table records no clinical significance for this variant.
Reference-table entries
PDXDC1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:15129970
- HGVS
- NM_015027.4,c.2205A>G,p.Leu735Leu
- Allele change
- Synonymous_L720L
Associated conditions / phenotypes
Synonymous_L735L|Silent|Synonymous_L707L|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.