Variant (rsID / SNP)

rs10407911

rs10407911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF577. Location: chromosome 19, position 52,376,119. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF577Not classified

Variant type: missense_variant
Chromosome / position: 19:52376119
HGVS: NM_001370447.1,c.1124C>T,p.Thr375Ile
Allele change: Silent

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.