Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs12919587

ZNF500

rs12919587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF500. Location: chromosome 16, position 4,815,602. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

ZNF500Not classified
Variant type
synonymous_variant
Chromosome / position
16:4815602
HGVS
NM_021646.4,c.378A>G,p.Glu126Glu
Allele change
Synonymous_E126E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.