Variant (rsID / SNP)

rs17697324

rs17697324 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DUXB. Location: chromosome 16, position 75,728,368. The table records no clinical significance for this variant.

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Reference-table entries

DUXBNot classified

Variant type: missense_variant
Chromosome / position: 16:75728368
HGVS: NM_001351307.2,c.497T>C,p.Met166Thr
Allele change: Missense_M79T

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.