Variant (rsID / SNP)

rs74597329

rs74597329 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNL3, IFNL4. Location: chromosome 19, position 39,739,155. The table records no clinical significance for this variant.

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Reference-table entries

IFNL3Not classified

Variant type: upstream_gene_variant
Chromosome / position: 19:39739155
HGVS: NM_001346937.2,c.-3438A>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.