Variant (rsID / SNP)

rs1978619

rs1978619 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF888. Location: chromosome 19, position 53,426,826. The table records no clinical significance for this variant.

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Reference-table entries

ZNF888Not classified

Variant type: upstream_gene_variant
Chromosome / position: 19:53426826
HGVS: NM_001384652.1,c.-369A>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.