Variant (rsID / SNP)

rs11883343

rs11883343 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF530. Location: chromosome 19, position 58,117,399. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF530Not classified

Variant type: missense_variant
Chromosome / position: 19:58117399
HGVS: NM_020880.5,c.506C>T,p.Thr169Met
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.