Variant (rsID / SNP)

rs3746319

rs3746319 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF224. Location: chromosome 19, position 44,612,231. The table records no clinical significance for this variant.

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Reference-table entries

ZNF224Not classified

Variant type: missense_variant
Chromosome / position: 19:44612231
HGVS: NM_001321645.3,c.1918A>G,p.Lys640Glu
Allele change: Missense_K640E

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.