Variant (rsID / SNP)

rs439676

rs439676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF221. Location: chromosome 19, position 44,470,420. The table records no clinical significance for this variant.

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Reference-table entries

ZNF221Not classified

Variant type: missense_variant
Chromosome / position: 19:44470420
HGVS: NM_001297588.2,c.766T>C,p.Cys256Arg
Allele change: Missense_C256R

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.