Variant (rsID / SNP)

rs201644342

rs201644342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS17. Location: chromosome 15, position 100,537,660. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ADAMTS17Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:100537660
Cytoband: 15q26.3
HGVS: NM_139057.4(ADAMTS17):c.2726G>A (p.Arg909Gln)
Allele change: Missense_R909Q

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.