Variant (rsID / SNP)

rs3792293

rs3792293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDCD10, SERPINI1. Location: chromosome 3, position 167,452,504. Clinical significance in the table: Benign.

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Reference-table entries

PDCD10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:167452504
Cytoband: 3q26.1
HGVS: NM_007217.4(PDCD10):c.-308T>C
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.