Variant (rsID / SNP)
rs56251528
rs56251528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS1. Location: chromosome 21, position 28,210,854. The table records no clinical significance for this variant.
Reference-table entries
ADAMTS1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 21:28210854
- HGVS
- NM_006988.5,c.2108G>A,p.Arg703His
- Allele change
- Missense_R703H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.