Variant (rsID / SNP)

rs10422063

rs10422063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF443. Location: chromosome 19, position 12,541,532. The table records no clinical significance for this variant.

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Reference-table entries

ZNF443Not classified

Variant type: missense_variant
Chromosome / position: 19:12541532
HGVS: NM_005815.5,c.1454G>T,p.Cys485Phe
Allele change: Missense_C485F

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.