Variant (rsID / SNP)

rs4717205

rs4717205 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF107. Location: chromosome 7, position 64,169,019. The table records no clinical significance for this variant.

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Reference-table entries

ZNF107Not classified

Variant type: synonymous_variant
Chromosome / position: 7:64169019
HGVS: NM_001388025.1,c.2676G>A,p.Glu892Glu
Allele change: Synonymous_E779E

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.