Variant (rsID / SNP)

rs113649109

rs113649109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAM9. Location: chromosome 8, position 38,879,190. Clinical significance in the table: Benign.

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Reference-table entries

ADAM9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:38879190
Cytoband: 8p11.22
HGVS: NM_003816.3(ADAM9):c.701C>T (p.Ala234Val)
Allele change: Silent

Associated conditions / phenotypes

Cone-rod dystrophy 9

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.