Variant (rsID / SNP)

rs3746414

rs3746414 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFP64. Location: chromosome 20, position 50,769,379. The table records no clinical significance for this variant.

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Reference-table entries

ZFP64Not classified

Variant type: missense_variant
Chromosome / position: 20:50769379
HGVS: NM_018197.3,c.1352G>A,p.Ser451Asn
Allele change: Silent

Associated conditions / phenotypes

Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of

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.