Variant (rsID / SNP)

rs17433780

rs17433780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBP3. Location: chromosome 1, position 89,474,818. The table records no clinical significance for this variant.

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Reference-table entries

GBP3Not classified

Variant type: missense_variant
Chromosome / position: 1:89474818
HGVS: NM_018284.3,c.1471T>C,p.Cys491Arg
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.