Variant (rsID / SNP)

rs799193

rs799193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF441. Location: chromosome 19, position 11,891,003. The table records no clinical significance for this variant.

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Reference-table entries

ZNF441Not classified

Variant type: missense_variant
Chromosome / position: 19:11891003
HGVS: NM_152355.3,c.364G>A,p.Val122Ile
Allele change: Missense_V122I

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.