Variant (rsID / SNP)

rs8104808

rs8104808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF880. Location: chromosome 19, position 52,887,427. The table records no clinical significance for this variant.

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Reference-table entries

ZNF880Not classified

Variant type: missense_variant
Chromosome / position: 19:52887427
HGVS: NM_001145434.2,c.594A>C,p.Arg198Ser
Allele change: Missense_R198S

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.