Variant (rsID / SNP)

rs144461893

rs144461893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DUOX1. Location: chromosome 15, position 45,457,004. The table records no clinical significance for this variant.

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Reference-table entries

DUOX1Not classified

Variant type: missense_variant
Chromosome / position: 15:45457004
HGVS: NM_017434.5,c.4561G>C,p.Gly1521Arg
Allele change: Missense_G1521R

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.