Variant (rsID / SNP)

rs2232866

rs2232866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UPB1. Location: chromosome 22, position 24,898,310. The table records no clinical significance for this variant.

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Reference-table entries

UPB1Not classified

Variant type: intron_variant
Chromosome / position: 22:24898310
HGVS: NM_016327.3,c.364+129C>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.