Variant (rsID / SNP)

rs873074

rs873074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SBNO2. Location: chromosome 19, position 1,174,602. The table records no clinical significance for this variant.

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Reference-table entries

SBNO2Not classified

Variant type: upstream_gene_variant
Chromosome / position: 19:1174602
HGVS: NM_014963.3,c.-558G>A

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.