Variant (rsID / SNP)

rs2054710

rs2054710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTSSB. Location: chromosome 3, position 161,090,616. The table records no clinical significance for this variant.

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Reference-table entries

SPTSSBNot classified

Variant type: upstream_gene_variant
Chromosome / position: 3:161090616
HGVS: NM_001040100.2,c.-1519G>A
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.