Variant (rsID / SNP)

rs7380824

rs7380824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STING1. Location: chromosome 5, position 138,856,982. The table records no clinical significance for this variant.

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Reference-table entries

STING1Not classified

Variant type: missense_variant
Chromosome / position: 5:138856982
HGVS: NM_198282.4,c.878G>A,p.Arg293Gln
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.