Variant (rsID / SNP)

rs9677004

rs9677004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF530. Location: chromosome 19, position 58,117,083. The table records no clinical significance for this variant.

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Reference-table entries

ZNF530Not classified

Variant type: missense_variant
Chromosome / position: 19:58117083
HGVS: NM_020880.5,c.190A>G,p.Thr64Ala
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.