Variant (rsID / SNP)

rs3745101

rs3745101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF701. Location: chromosome 19, position 53,085,813. The table records no clinical significance for this variant.

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Reference-table entries

ZNF701Not classified

Variant type: synonymous_variant
Chromosome / position: 19:53085813
HGVS: NM_001172655.1,c.699T>C,p.Ala233Ala
Allele change: Synonymous_A167A

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.