Variant (rsID / SNP)

rs6558541

rs6558541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIR3674. Location: chromosome 8, position 1,748,941. The table records no clinical significance for this variant.

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Reference-table entries

MIR3674Not classified

Variant type: upstream_gene_variant
Chromosome / position: 8:1748941
HGVS: NR_037445.1,n.-350A>G

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.