Variant (rsID / SNP)

rs61731605

rs61731605 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSCR8, DSCR4. Location: chromosome 21, position 39,493,232. The table records no clinical significance for this variant.

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Reference-table entries

DSCR8Not classified

Variant type: upstream_gene_variant
Chromosome / position: 21:39493232
HGVS: NR_026838.1,n.-313G>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.