Variant (rsID / SNP)

rs4891164

rs4891164 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF516. Location: chromosome 18, position 74,208,573. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF516Not classified

Variant type: upstream_gene_variant
Chromosome / position: 18:74208573
HGVS: NM_014643.4,c.-1745C>T
Allele change: Missense_R139K

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.