Variant (rsID / SNP)

rs966591

rs966591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF557. Location: chromosome 19, position 7,083,629. The table records no clinical significance for this variant.

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Reference-table entries

ZNF557Not classified

Variant type: synonymous_variant
Chromosome / position: 19:7083629
HGVS: NM_001044387.2,c.1167A>G,p.Ser389Ser
Allele change: Synonymous_S389S

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.