Variant (rsID / SNP)

rs4801478

rs4801478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF548. Location: chromosome 19, position 57,909,872. The table records no clinical significance for this variant.

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Reference-table entries

ZNF548Not classified

Variant type: missense_variant
Chromosome / position: 19:57909872
HGVS: NM_001172773.2,c.253G>A,p.Ala85Thr
Allele change: Missense_A73T

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.