Variant (rsID / SNP)

rs3785521

rs3785521 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B3GNTL1, TBCD. Location: chromosome 17, position 80,895,769. The table records no clinical significance for this variant.

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Reference-table entries

B3GNTL1Not classified

Variant type: downstream_gene_variant
Chromosome / position: 17:80895769
HGVS: NM_001320742.2,c.*6181T>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.