Variant (rsID / SNP)

rs1126828

rs1126828 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPN1. Location: chromosome 3, position 128,344,786. The table records no clinical significance for this variant.

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Reference-table entries

RPN1Not classified

Variant type: synonymous_variant
Chromosome / position: 3:128344786
HGVS: NM_002950.4,c.1206C>T,p.Asp402Asp
Allele change: Synonymous_D402D

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.