Variant (rsID / SNP)

rs10410539

rs10410539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF57. Location: chromosome 19, position 2,917,612. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF57Not classified

Variant type: synonymous_variant
Chromosome / position: 19:2917612
HGVS: NM_173480.3,c.993T>C,p.Thr331Thr
Allele change: Synonymous_T331T

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.