Variant (rsID / SNP)

rs8337

rs8337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBD. Location: chromosome 6, position 29,523,676. The table records no clinical significance for this variant.

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Reference-table entries

UBDNot classified

Variant type: missense_variant
Chromosome / position: 6:29523676
HGVS: NM_006398.4,c.479G>C,p.Cys160Ser
Allele change: Missense_C160S

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.