Variant (rsID / SNP)

rs13255694

rs13255694 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAM7. Location: chromosome 8, position 24,339,679. The table records no clinical significance for this variant.

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Reference-table entries

ADAM7Not classified

Variant type: missense_variant
Chromosome / position: 8:24339679
HGVS: NM_003817.4,c.730G>A,p.Val244Met
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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