Variant (rsID / SNP)

rs35103368

rs35103368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBN1. Location: chromosome 16, position 4,920,335. The table records no clinical significance for this variant.

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Reference-table entries

UBN1Not classified

Variant type: missense_variant
Chromosome / position: 16:4920335
HGVS: NM_001079514.3,c.1304A>G,p.Tyr435Cys
Allele change: Missense_Y435C

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.