Variant (rsID / SNP)

rs875622

rs875622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPS15L1. Location: chromosome 19, position 16,467,759. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EPS15L1Not classified

Variant type: downstream_gene_variant
Chromosome / position: 19:16467759
HGVS: NM_001258375.2,c.*5019T>C
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.