Variant (rsID / SNP)

rs4438413

rs4438413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF525. Location: chromosome 19, position 53,884,412. The table records no clinical significance for this variant.

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Reference-table entries

ZNF525Not classified

Variant type: missense_variant
Chromosome / position: 19:53884412
HGVS: NM_001348156.2,c.580G>A,p.Asp194Asn
Allele change: Missense_D194N

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.