Variant (rsID / SNP)

rs28620278

rs28620278 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF280D. Location: chromosome 15, position 56,959,028. The table records no clinical significance for this variant.

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Reference-table entries

ZNF280DNot classified

Variant type: missense_variant
Chromosome / position: 15:56959028
HGVS: NM_001288588.2,c.1702G>A,p.Val568Ile
Allele change: Missense_V568I

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.