Variant (rsID / SNP)

rs4719480

rs4719480 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGR2. Location: chromosome 7, position 16,834,551. The table records no clinical significance for this variant.

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Reference-table entries

AGR2Not classified

Variant type: intron_variant
Chromosome / position: 7:16834551
HGVS: NM_006408.4,c.478+9G>T
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.