Variant (rsID / SNP)

rs3745651

rs3745651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF490. Location: chromosome 19, position 12,692,001. The table records no clinical significance for this variant.

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Reference-table entries

ZNF490Not classified

Variant type: synonymous_variant
Chromosome / position: 19:12692001
HGVS: NM_020714.3,c.888C>T,p.His296His
Allele change: Synonymous_H296H

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.