Variant (rsID / SNP)

rs4805162

rs4805162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF565. Location: chromosome 19, position 36,674,305. The table records no clinical significance for this variant.

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Reference-table entries

ZNF565Not classified

Variant type: missense_variant
Chromosome / position: 19:36674305
HGVS: NM_001042474.2,c.563T>C,p.Ile188Thr
Allele change: Missense_I188T

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.