Variant (rsID / SNP)

rs1243464

rs1243464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASE13, NDRG2. Location: chromosome 14, position 21,504,447. The table records no clinical significance for this variant.

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Reference-table entries

RNASE13Not classified

Variant type: upstream_gene_variant
Chromosome / position: 14:21504447
HGVS: NM_001012264.4,c.-1641T>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.