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Variant (rsID / SNP)

rs428785

ADAMTS1

rs428785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS1. Location: chromosome 21, position 28,216,595. The table records no clinical significance for this variant.

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Reference-table entries

ADAMTS1Not classified
Variant type
missense_variant
Chromosome / position
21:28216595
HGVS
NM_006988.5,c.679G>C,p.Ala227Pro
Allele change
Missense_A227P

Associated conditions / phenotypes

Pelvic Organ Prolapse

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.