Variant (rsID / SNP)

rs4801959

rs4801959 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF665. Location: chromosome 19, position 53,669,273. The table records no clinical significance for this variant.

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Reference-table entries

ZNF665Not classified

Variant type: missense_variant
Chromosome / position: 19:53669273
HGVS: NM_001353458.2,c.554A>G,p.His185Arg
Allele change: Missense_H157R

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.