Variant (rsID / SNP)

rs3746222

rs3746222 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF416. Location: chromosome 19, position 58,084,930. The table records no clinical significance for this variant.

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Reference-table entries

ZNF416Not classified

Variant type: synonymous_variant
Chromosome / position: 19:58084930
HGVS: NM_017879.3,c.342C>T,p.Thr114Thr
Allele change: Synonymous_T114T

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.